Canonical Allele Identifier: CA2210140961

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154950C= , CM000678.2:g.16154950C=	GRCh38
NC_000016.9:g.16248807C= , CM000678.1:g.16248807C=	GRCh37
NC_000016.8:g.16156308C=	NCBI36
NG_007558.2:g.73522G=
NG_007558.3:g.73668G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.827G=
ENST00000622290.5:c.*136G=	ENSP00000483331.2:n.*136G=
ENST00000205557.12:c.3964G= MANE Select	ENSP00000205557.7:p.Gly1322=
ENST00000640696.1:c.778G=	ENSP00000492197.1:p.Gly260=
ENST00000205557.11:c.3964G=	ENSP00000205557.7:p.Gly1322=
ENST00000456970.6:c.3589G=	ENSP00000405002.2:n.3589G=
ENST00000576204.5:n.827G=
ENST00000622290.4:c.*1173G=	ENSP00000483331.1:n.*1173G=
NM_001171.5:c.3964G=	NP_001162.4:p.Gly1322=
XM_011522479.1:c.3931G=	XP_011520781.1:p.Gly1311=
XM_011522480.1:c.3622G=	XP_011520782.1:p.Gly1208=
XM_011522481.1:c.3622G=	XP_011520783.1:p.Gly1208=
XR_932836.1:n.4262G=
XR_932837.1:n.4000G=
XR_932838.1:n.4063G=
XR_933134.1:n.539-4831C=
NM_001351800.1:c.3622G=	NP_001338729.1:p.Gly1208=
NR_147784.1:n.3626G=
XM_011522479.2:c.3931G=	XP_011520781.1:p.Gly1311=
XM_011522481.3:c.3622G=	XP_011520783.1:p.Gly1208=
XM_017023212.1:c.3796G=	XP_016878701.1:p.Gly1266=
XM_024450261.1:c.4000G=	XP_024306029.1:p.Gly1334=
XR_932837.3:n.3945G=
NM_001171.6:c.3964G= MANE Select	NP_001162.5:p.Gly1322=