Canonical Allele Identifier: CA2210131549

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159426G= , CM000678.2:g.16159426G=	GRCh38
NC_000016.9:g.16253283G= , CM000678.1:g.16253283G=	GRCh37
NC_000016.8:g.16160784G=	NCBI36
NG_007558.2:g.69046C=
NG_007558.3:g.69192C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.3735+56C=	ENSP00000483331.2:n.3735+56C=
ENST00000205557.12:c.3735+56C= MANE Select	ENSP00000205557.7:n.3735+56C=
ENST00000640696.1:c.549+56C=	ENSP00000492197.1:n.549+56C=
ENST00000205557.11:c.3735+56C=	ENSP00000205557.7:n.3735+56C=
ENST00000456970.6:c.3360+56C=	ENSP00000405002.2:n.3360+56C=
ENST00000622290.4:c.*944+56C=	ENSP00000483331.1:n.*944+56C=
NM_001171.5:c.3735+56C=	NP_001162.4:n.3735+56C=
XM_011522479.1:c.3702+56C=	XP_011520781.1:n.3702+56C=
XM_011522480.1:c.3393+56C=	XP_011520782.1:n.3393+56C=
XM_011522481.1:c.3393+56C=	XP_011520783.1:n.3393+56C=
XR_932836.1:n.3970+56C=
XR_932837.1:n.3771+56C=
XR_932838.1:n.3771+56C=
XR_933134.1:n.539-355G=
NM_001351800.1:c.3393+56C=	NP_001338729.1:n.3393+56C=
NR_147784.1:n.3397+56C=
XM_011522479.2:c.3702+56C=	XP_011520781.1:n.3702+56C=
XM_011522481.3:c.3393+56C=	XP_011520783.1:n.3393+56C=
XM_017023212.1:c.3567+56C=	XP_016878701.1:n.3567+56C=
XM_024450261.1:c.3771+56C=	XP_024306029.1:n.3771+56C=
XR_932836.2:n.3916+56C=
XR_932837.3:n.3716+56C=
XR_932838.3:n.3716+56C=
NM_001171.6:c.3735+56C= MANE Select	NP_001162.5:n.3735+56C=