Canonical Allele Identifier: CA2210140742

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154831A= , CM000678.2:g.16154831A=	GRCh38
NC_000016.9:g.16248688A= , CM000678.1:g.16248688A=	GRCh37
NC_000016.8:g.16156189A=	NCBI36
NG_007558.2:g.73641T=
NG_007558.3:g.73787T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.905-37T=
ENST00000622290.5:c.*214-37T=	ENSP00000483331.2:n.*214-37T=
ENST00000205557.12:c.4042-37T= MANE Select	ENSP00000205557.7:n.4042-37T=
ENST00000640696.1:c.856-37T=	ENSP00000492197.1:n.856-37T=
ENST00000205557.11:c.4042-37T=	ENSP00000205557.7:n.4042-37T=
ENST00000456970.6:c.3667-37T=	ENSP00000405002.2:n.3667-37T=
ENST00000576204.5:n.905-37T=
ENST00000622290.4:c.*1251-37T=	ENSP00000483331.1:n.*1251-37T=
NM_001171.5:c.4042-37T=	NP_001162.4:n.4042-37T=
XM_011522479.1:c.4009-37T=	XP_011520781.1:n.4009-37T=
XM_011522480.1:c.3700-37T=	XP_011520782.1:n.3700-37T=
XM_011522481.1:c.3700-37T=	XP_011520783.1:n.3700-37T=
XR_933134.1:n.539-4950A=
NM_001351800.1:c.3700-37T=	NP_001338729.1:n.3700-37T=
NR_147784.1:n.3704-37T=
XM_011522479.2:c.4009-37T=	XP_011520781.1:n.4009-37T=
XM_011522481.3:c.3700-37T=	XP_011520783.1:n.3700-37T=
XM_017023212.1:c.3874-37T=	XP_016878701.1:n.3874-37T=
XM_024450261.1:c.4078-37T=	XP_024306029.1:n.4078-37T=
NM_001171.6:c.4042-37T= MANE Select	NP_001162.5:n.4042-37T=