Canonical Allele Identifier: CA2210132067

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159581C= , CM000678.2:g.16159581C=	GRCh38
NC_000016.9:g.16253438C= , CM000678.1:g.16253438C=	GRCh37
NC_000016.8:g.16160939C=	NCBI36
NG_007558.2:g.68891G=
NG_007558.3:g.69037G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3636G=	ENSP00000483331.2:p.Val1212=
ENST00000205557.12:c.3636G= MANE Select	ENSP00000205557.7:p.Val1212=
ENST00000640696.1:c.450G=	ENSP00000492197.1:p.Val150=
ENST00000205557.11:c.3636G=	ENSP00000205557.7:p.Val1212=
ENST00000456970.6:c.3261G=	ENSP00000405002.2:n.3261G=
ENST00000622290.4:c.*845G=	ENSP00000483331.1:n.*845G=
NM_001171.5:c.3636G=	NP_001162.4:p.Val1212=
XM_011522479.1:c.3603G=	XP_011520781.1:p.Val1201=
XM_011522480.1:c.3294G=	XP_011520782.1:p.Val1098=
XM_011522481.1:c.3294G=	XP_011520783.1:p.Val1098=
XR_932836.1:n.3871G=
XR_932837.1:n.3672G=
XR_932838.1:n.3672G=
XR_933134.1:n.539-200C=
NM_001351800.1:c.3294G=	NP_001338729.1:p.Val1098=
NR_147784.1:n.3298G=
XM_011522479.2:c.3603G=	XP_011520781.1:p.Val1201=
XM_011522481.3:c.3294G=	XP_011520783.1:p.Val1098=
XM_017023212.1:c.3468G=	XP_016878701.1:p.Val1156=
XM_024450261.1:c.3672G=	XP_024306029.1:p.Val1224=
XR_932836.2:n.3817G=
XR_932837.3:n.3617G=
XR_932838.3:n.3617G=
NM_001171.6:c.3636G= MANE Select	NP_001162.5:p.Val1212=