Canonical Allele Identifier: CA2557682656
Gene: CCDC149 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24821251_24821252insTACAGTTTATATT , CM000666.2:g.24821251_24821252insTACAGTTTATATT GRCh38
NC_000004.11:g.24822873_24822874insTACAGTTTATATT , CM000666.1:g.24822873_24822874insTACAGTTTATATT GRCh37
NC_000004.10:g.24431971_24431972insTACAGTTTATATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635206.3:c.1028-165_1028-164insAATATAAACTGTA MANE Select ENSP00000488929.2:n.1028-165_1028-164insAATATAAACTGTA
ENST00000635206.2:c.1043-165_1043-164insAATATAAACTGTA ENSP00000488929.1:n.1043-165_1043-164insAATATAAACTGTA
ENST00000389609.8:c.1042+1245_1042+1246insAATATAAACTGTA ENSP00000374260.4:n.1042+1245_1042+1246insAATATAAACTGTA
ENST00000502801.1:c.373-12433_373-12432insAATATAAACTGTA ENSP00000427529.1:n.373-12433_373-12432insAATATAAACTGTA
ENST00000504487.5:c.1042+1245_1042+1246insAATATAAACTGTA ENSP00000425715.1:n.1042+1245_1042+1246insAATATAAACTGTA
ENST00000508236.1:n.550-165_550-164insAATATAAACTGTA
ENST00000635206.1:c.1043-165_1043-164insAATATAAACTGTA ENSP00000488929.1:n.1043-165_1043-164insAATATAAACTGTA
NM_001130726.2:c.1042+1245_1042+1246insAATATAAACTGTA NP_001124198.1:n.1042+1245_1042+1246insAATATAAACTGTA
NM_173463.4:c.1042+1245_1042+1246insAATATAAACTGTA NP_775734.2:n.1042+1245_1042+1246insAATATAAACTGTA
XM_005248210.2:c.1043-165_1043-164insAATATAAACTGTA XP_005248267.1:n.1043-165_1043-164insAATATAAACTGTA
XM_011513906.1:c.1043-165_1043-164insAATATAAACTGTA XP_011512208.1:n.1043-165_1043-164insAATATAAACTGTA
XM_011513907.1:c.878-165_878-164insAATATAAACTGTA XP_011512209.1:n.878-165_878-164insAATATAAACTGTA
XM_011513908.1:c.878-165_878-164insAATATAAACTGTA XP_011512210.1:n.878-165_878-164insAATATAAACTGTA
NM_001130726.3:c.1042+1245_1042+1246insAATATAAACTGTA NP_001124198.1:n.1042+1245_1042+1246insAATATAAACTGTA
NM_001330643.1:c.1043-165_1043-164insAATATAAACTGTA NP_001317572.1:n.1043-165_1043-164insAATATAAACTGTA
NM_001330644.1:c.877+1245_877+1246insAATATAAACTGTA NP_001317573.1:n.877+1245_877+1246insAATATAAACTGTA
NM_173463.5:c.1042+1245_1042+1246insAATATAAACTGTA NP_775734.2:n.1042+1245_1042+1246insAATATAAACTGTA
XM_011513906.3:c.1043-165_1043-164insAATATAAACTGTA XP_011512208.1:n.1043-165_1043-164insAATATAAACTGTA
XM_011513907.3:c.878-165_878-164insAATATAAACTGTA XP_011512209.1:n.878-165_878-164insAATATAAACTGTA
XM_011513908.2:c.878-165_878-164insAATATAAACTGTA XP_011512210.1:n.878-165_878-164insAATATAAACTGTA
XM_017008827.2:c.1042+1245_1042+1246insAATATAAACTGTA XP_016864316.1:n.1042+1245_1042+1246insAATATAAACTGTA
NM_001130726.4:c.1042+1245_1042+1246insAATATAAACTGTA NP_001124198.1:n.1042+1245_1042+1246insAATATAAACTGTA
NM_001330643.2:c.1043-165_1043-164insAATATAAACTGTA NP_001317572.1:n.1043-165_1043-164insAATATAAACTGTA
NM_001330644.2:c.877+1245_877+1246insAATATAAACTGTA NP_001317573.1:n.877+1245_877+1246insAATATAAACTGTA
NM_173463.6:c.1042+1245_1042+1246insAATATAAACTGTA NP_775734.2:n.1042+1245_1042+1246insAATATAAACTGTA
NM_001130726.5:c.1027+1245_1027+1246insAATATAAACTGTA NP_001124198.2:n.1027+1245_1027+1246insAATATAAACTGTA
NM_001395273.1:c.1028-165_1028-164insAATATAAACTGTA MANE Select NP_001382202.1:n.1028-165_1028-164insAATATAAACTGTA