Canonical Allele Identifier: CA2210131803

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159504T= , CM000678.2:g.16159504T=	GRCh38
NC_000016.9:g.16253361T= , CM000678.1:g.16253361T=	GRCh37
NC_000016.8:g.16160862T=	NCBI36
NG_007558.2:g.68968A=
NG_007558.3:g.69114A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3713A=	ENSP00000483331.2:p.Asp1238=
ENST00000205557.12:c.3713A= MANE Select	ENSP00000205557.7:p.Asp1238=
ENST00000640696.1:c.527A=	ENSP00000492197.1:p.Asp176=
ENST00000205557.11:c.3713A=	ENSP00000205557.7:p.Asp1238=
ENST00000456970.6:c.3338A=	ENSP00000405002.2:n.3338A=
ENST00000622290.4:c.*922A=	ENSP00000483331.1:n.*922A=
NM_001171.5:c.3713A=	NP_001162.4:p.Asp1238=
XM_011522479.1:c.3680A=	XP_011520781.1:p.Asp1227=
XM_011522480.1:c.3371A=	XP_011520782.1:p.Asp1124=
XM_011522481.1:c.3371A=	XP_011520783.1:p.Asp1124=
XR_932836.1:n.3948A=
XR_932837.1:n.3749A=
XR_932838.1:n.3749A=
XR_933134.1:n.539-277T=
NM_001351800.1:c.3371A=	NP_001338729.1:p.Asp1124=
NR_147784.1:n.3375A=
XM_011522479.2:c.3680A=	XP_011520781.1:p.Asp1227=
XM_011522481.3:c.3371A=	XP_011520783.1:p.Asp1124=
XM_017023212.1:c.3545A=	XP_016878701.1:p.Asp1182=
XM_024450261.1:c.3749A=	XP_024306029.1:p.Asp1250=
XR_932836.2:n.3894A=
XR_932837.3:n.3694A=
XR_932838.3:n.3694A=
NM_001171.6:c.3713A= MANE Select	NP_001162.5:p.Asp1238=