Canonical Allele Identifier: CA1445083434
Gene: CCDC149 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24821203_24821204delinsAC , CM000666.2:g.24821203_24821204delinsAC GRCh38
NC_000004.11:g.24822825_24822826delinsAC , CM000666.1:g.24822825_24822826delinsAC GRCh37
NC_000004.10:g.24431923_24431924delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635206.3:c.1028-117_1028-116delinsGT MANE Select ENSP00000488929.2:n.1028-117_1028-116delinsGT
ENST00000635206.2:c.1043-117_1043-116delinsGT ENSP00000488929.1:n.1043-117_1043-116delinsGT
ENST00000389609.8:c.1043-1229_1043-1228delinsGT ENSP00000374260.4:n.1043-1229_1043-1228delinsGT
ENST00000502801.1:c.373-12385_373-12384delinsGT ENSP00000427529.1:n.373-12385_373-12384delinsGT
ENST00000504487.5:c.1043-1229_1043-1228delinsGT ENSP00000425715.1:n.1043-1229_1043-1228delinsGT
ENST00000508236.1:n.550-117_550-116delinsGT
ENST00000635206.1:c.1043-117_1043-116delinsGT ENSP00000488929.1:n.1043-117_1043-116delinsGT
NM_001130726.2:c.1043-1229_1043-1228delinsGT NP_001124198.1:n.1043-1229_1043-1228delinsGT
NM_173463.4:c.1043-1229_1043-1228delinsGT NP_775734.2:n.1043-1229_1043-1228delinsGT
XM_005248210.2:c.1043-117_1043-116delinsGT XP_005248267.1:n.1043-117_1043-116delinsGT
XM_011513906.1:c.1043-117_1043-116delinsGT XP_011512208.1:n.1043-117_1043-116delinsGT
XM_011513907.1:c.878-117_878-116delinsGT XP_011512209.1:n.878-117_878-116delinsGT
XM_011513908.1:c.878-117_878-116delinsGT XP_011512210.1:n.878-117_878-116delinsGT
NM_001130726.3:c.1043-1229_1043-1228delinsGT NP_001124198.1:n.1043-1229_1043-1228delinsGT
NM_001330643.1:c.1043-117_1043-116delinsGT NP_001317572.1:n.1043-117_1043-116delinsGT
NM_001330644.1:c.878-1229_878-1228delinsGT NP_001317573.1:n.878-1229_878-1228delinsGT
NM_173463.5:c.1043-1229_1043-1228delinsGT NP_775734.2:n.1043-1229_1043-1228delinsGT
XM_011513906.3:c.1043-117_1043-116delinsGT XP_011512208.1:n.1043-117_1043-116delinsGT
XM_011513907.3:c.878-117_878-116delinsGT XP_011512209.1:n.878-117_878-116delinsGT
XM_011513908.2:c.878-117_878-116delinsGT XP_011512210.1:n.878-117_878-116delinsGT
XM_017008827.2:c.1043-1229_1043-1228delinsGT XP_016864316.1:n.1043-1229_1043-1228delinsGT
NM_001130726.4:c.1043-1229_1043-1228delinsGT NP_001124198.1:n.1043-1229_1043-1228delinsGT
NM_001330643.2:c.1043-117_1043-116delinsGT NP_001317572.1:n.1043-117_1043-116delinsGT
NM_001330644.2:c.878-1229_878-1228delinsGT NP_001317573.1:n.878-1229_878-1228delinsGT
NM_173463.6:c.1043-1229_1043-1228delinsGT NP_775734.2:n.1043-1229_1043-1228delinsGT
NM_001130726.5:c.1028-1229_1028-1228delinsGT NP_001124198.2:n.1028-1229_1028-1228delinsGT
NM_001395273.1:c.1028-117_1028-116delinsGT MANE Select NP_001382202.1:n.1028-117_1028-116delinsGT