Canonical Allele Identifier: CA2210132016

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159557A= , CM000678.2:g.16159557A=	GRCh38
NC_000016.9:g.16253414A= , CM000678.1:g.16253414A=	GRCh37
NC_000016.8:g.16160915A=	NCBI36
NG_007558.2:g.68915T=
NG_007558.3:g.69061T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3660T=	ENSP00000483331.2:p.Val1220=
ENST00000205557.12:c.3660T= MANE Select	ENSP00000205557.7:p.Val1220=
ENST00000640696.1:c.474T=	ENSP00000492197.1:p.Val158=
ENST00000205557.11:c.3660T=	ENSP00000205557.7:p.Val1220=
ENST00000456970.6:c.3285T=	ENSP00000405002.2:n.3285T=
ENST00000622290.4:c.*869T=	ENSP00000483331.1:n.*869T=
NM_001171.5:c.3660T=	NP_001162.4:p.Val1220=
XM_011522479.1:c.3627T=	XP_011520781.1:p.Val1209=
XM_011522480.1:c.3318T=	XP_011520782.1:p.Val1106=
XM_011522481.1:c.3318T=	XP_011520783.1:p.Val1106=
XR_932836.1:n.3895T=
XR_932837.1:n.3696T=
XR_932838.1:n.3696T=
XR_933134.1:n.539-224A=
NM_001351800.1:c.3318T=	NP_001338729.1:p.Val1106=
NR_147784.1:n.3322T=
XM_011522479.2:c.3627T=	XP_011520781.1:p.Val1209=
XM_011522481.3:c.3318T=	XP_011520783.1:p.Val1106=
XM_017023212.1:c.3492T=	XP_016878701.1:p.Val1164=
XM_024450261.1:c.3696T=	XP_024306029.1:p.Val1232=
XR_932836.2:n.3841T=
XR_932837.3:n.3641T=
XR_932838.3:n.3641T=
NM_001171.6:c.3660T= MANE Select	NP_001162.5:p.Val1220=