Canonical Allele Identifier: CA793277411
Gene: CCDC149 HGNC NCBI

Linked Data

dbSNP Id: rs1018895466
MyVariant Identifiers: chr4:g.24822894A>C (hg19) chr4:g.24821272A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24821272A>C , CM000666.2:g.24821272A>C GRCh38
NC_000004.11:g.24822894A>C , CM000666.1:g.24822894A>C GRCh37
NC_000004.10:g.24431992A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635206.3:c.1028-185T>G MANE Select ENSP00000488929.2:n.1028-185T>G
ENST00000635206.2:c.1043-185T>G ENSP00000488929.1:n.1043-185T>G
ENST00000389609.8:c.1042+1225T>G ENSP00000374260.4:n.1042+1225T>G
ENST00000502801.1:c.373-12453T>G ENSP00000427529.1:n.373-12453T>G
ENST00000504487.5:c.1042+1225T>G ENSP00000425715.1:n.1042+1225T>G
ENST00000508236.1:n.550-185T>G
ENST00000635206.1:c.1043-185T>G ENSP00000488929.1:n.1043-185T>G
NM_001130726.2:c.1042+1225T>G NP_001124198.1:n.1042+1225T>G
NM_173463.4:c.1042+1225T>G NP_775734.2:n.1042+1225T>G
XM_005248210.2:c.1043-185T>G XP_005248267.1:n.1043-185T>G
XM_011513906.1:c.1043-185T>G XP_011512208.1:n.1043-185T>G
XM_011513907.1:c.878-185T>G XP_011512209.1:n.878-185T>G
XM_011513908.1:c.878-185T>G XP_011512210.1:n.878-185T>G
NM_001130726.3:c.1042+1225T>G NP_001124198.1:n.1042+1225T>G
NM_001330643.1:c.1043-185T>G NP_001317572.1:n.1043-185T>G
NM_001330644.1:c.877+1225T>G NP_001317573.1:n.877+1225T>G
NM_173463.5:c.1042+1225T>G NP_775734.2:n.1042+1225T>G
XM_011513906.3:c.1043-185T>G XP_011512208.1:n.1043-185T>G
XM_011513907.3:c.878-185T>G XP_011512209.1:n.878-185T>G
XM_011513908.2:c.878-185T>G XP_011512210.1:n.878-185T>G
XM_017008827.2:c.1042+1225T>G XP_016864316.1:n.1042+1225T>G
NM_001130726.4:c.1042+1225T>G NP_001124198.1:n.1042+1225T>G
NM_001330643.2:c.1043-185T>G NP_001317572.1:n.1043-185T>G
NM_001330644.2:c.877+1225T>G NP_001317573.1:n.877+1225T>G
NM_173463.6:c.1042+1225T>G NP_775734.2:n.1042+1225T>G
NM_001130726.5:c.1027+1225T>G NP_001124198.2:n.1027+1225T>G
NM_001395273.1:c.1028-185T>G MANE Select NP_001382202.1:n.1028-185T>G
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