Canonical Allele Identifier: CA2210140506

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154684C= , CM000678.2:g.16154684C=	GRCh38
NC_000016.9:g.16248541C= , CM000678.1:g.16248541C=	GRCh37
NC_000016.8:g.16156042C=	NCBI36
NG_007558.2:g.73788G=
NG_007558.3:g.73934G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.*324G=	ENSP00000483331.2:n.*324G=
ENST00000205557.12:c.4152G= MANE Select	ENSP00000205557.7:p.Val1384=
ENST00000640696.1:c.966G=	ENSP00000492197.1:p.Val322=
ENST00000205557.11:c.4152G=	ENSP00000205557.7:p.Val1384=
ENST00000456970.6:c.3777G=	ENSP00000405002.2:n.3777G=
ENST00000576204.5:n.1015G=
ENST00000622290.4:c.*1361G=	ENSP00000483331.1:n.*1361G=
NM_001171.5:c.4152G=	NP_001162.4:p.Val1384=
XM_011522479.1:c.4119G=	XP_011520781.1:p.Val1373=
XM_011522480.1:c.3810G=	XP_011520782.1:p.Val1270=
XM_011522481.1:c.3810G=	XP_011520783.1:p.Val1270=
XR_933134.1:n.539-5097C=
NM_001351800.1:c.3810G=	NP_001338729.1:p.Val1270=
NR_147784.1:n.3814G=
XM_011522479.2:c.4119G=	XP_011520781.1:p.Val1373=
XM_011522481.3:c.3810G=	XP_011520783.1:p.Val1270=
XM_017023212.1:c.3984G=	XP_016878701.1:p.Val1328=
XM_024450261.1:c.4188G=	XP_024306029.1:p.Val1396=
NM_001171.6:c.4152G= MANE Select	NP_001162.5:p.Val1384=