Canonical Allele Identifier: CA2210131521

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159413A= , CM000678.2:g.16159413A=	GRCh38
NC_000016.9:g.16253270A= , CM000678.1:g.16253270A=	GRCh37
NC_000016.8:g.16160771A=	NCBI36
NG_007558.2:g.69059T=
NG_007558.3:g.69205T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.3735+69T=	ENSP00000483331.2:n.3735+69T=
ENST00000205557.12:c.3735+69T= MANE Select	ENSP00000205557.7:n.3735+69T=
ENST00000640696.1:c.549+69T=	ENSP00000492197.1:n.549+69T=
ENST00000205557.11:c.3735+69T=	ENSP00000205557.7:n.3735+69T=
ENST00000456970.6:c.3360+69T=	ENSP00000405002.2:n.3360+69T=
ENST00000622290.4:c.*944+69T=	ENSP00000483331.1:n.*944+69T=
NM_001171.5:c.3735+69T=	NP_001162.4:n.3735+69T=
XM_011522479.1:c.3702+69T=	XP_011520781.1:n.3702+69T=
XM_011522480.1:c.3393+69T=	XP_011520782.1:n.3393+69T=
XM_011522481.1:c.3393+69T=	XP_011520783.1:n.3393+69T=
XR_932836.1:n.3970+69T=
XR_932837.1:n.3771+69T=
XR_932838.1:n.3771+69T=
XR_933134.1:n.539-368A=
NM_001351800.1:c.3393+69T=	NP_001338729.1:n.3393+69T=
NR_147784.1:n.3397+69T=
XM_011522479.2:c.3702+69T=	XP_011520781.1:n.3702+69T=
XM_011522481.3:c.3393+69T=	XP_011520783.1:n.3393+69T=
XM_017023212.1:c.3567+69T=	XP_016878701.1:n.3567+69T=
XM_024450261.1:c.3771+69T=	XP_024306029.1:n.3771+69T=
XR_932836.2:n.3916+69T=
XR_932837.3:n.3716+69T=
XR_932838.3:n.3716+69T=
NM_001171.6:c.3735+69T= MANE Select	NP_001162.5:n.3735+69T=