Canonical Allele Identifier: CA394884355

Gene: ABCC6

Linked Data

• COSMIC: COSM6213656
• MyVariant Identifiers: chr16:g.16248497C>T (hg19) ; chr16:g.16154640C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154640C>T , CM000678.2:g.16154640C>T	GRCh38
NC_000016.9:g.16248497C>T , CM000678.1:g.16248497C>T	GRCh37
NC_000016.8:g.16155998C>T	NCBI36
NG_007558.2:g.73832G>A
NG_007558.3:g.73978G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*368G>A	ENSP00000483331.2:n.*368G>A
ENST00000205557.12:c.4196G>A MANE Select	ENSP00000205557.7:p.Gly1399Asp
ENST00000640696.1:c.1010G>A	ENSP00000492197.1:p.Gly337Asp
ENST00000205557.11:c.4196G>A	ENSP00000205557.7:p.Gly1399Asp
ENST00000456970.6:c.3821G>A	ENSP00000405002.2:n.3821G>A
ENST00000576204.5:n.1059G>A
ENST00000622290.4:c.*1405G>A	ENSP00000483331.1:n.*1405G>A
NM_001171.5:c.4196G>A	NP_001162.4:p.Gly1399Asp
XM_011522479.1:c.4163G>A	XP_011520781.1:p.Gly1388Asp
XM_011522480.1:c.3854G>A	XP_011520782.1:p.Gly1285Asp
XM_011522481.1:c.3854G>A	XP_011520783.1:p.Gly1285Asp
XR_933134.1:n.539-5141C>T
NM_001351800.1:c.3854G>A	NP_001338729.1:p.Gly1285Asp
NR_147784.1:n.3858G>A
XM_011522479.2:c.4163G>A	XP_011520781.1:p.Gly1388Asp
XM_011522481.3:c.3854G>A	XP_011520783.1:p.Gly1285Asp
XM_017023212.1:c.4028G>A	XP_016878701.1:p.Gly1343Asp
XM_024450261.1:c.4232G>A	XP_024306029.1:p.Gly1411Asp
NM_001171.6:c.4196G>A MANE Select	NP_001162.5:p.Gly1399Asp