Canonical Allele Identifier: CA2210139879

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16165692C= , CM000678.2:g.16165692C=	GRCh38
NC_000016.9:g.16259549C= , CM000678.1:g.16259549C=	GRCh37
NC_000016.8:g.16167050C=	NCBI36
NG_007558.2:g.62780G=
NG_007558.3:g.62926G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3237G=	ENSP00000483331.2:p.Val1079=
ENST00000205557.12:c.3237G= MANE Select	ENSP00000205557.7:p.Val1079=
ENST00000640696.1:c.252G=	ENSP00000492197.1:p.Val84=
ENST00000205557.11:c.3237G=	ENSP00000205557.7:p.Val1079=
ENST00000456970.6:c.3062G=	ENSP00000405002.2:n.3062G=
ENST00000622290.4:c.*446G=	ENSP00000483331.1:n.*446G=
NM_001171.5:c.3237G=	NP_001162.4:p.Val1079=
XM_011522479.1:c.3204G=	XP_011520781.1:p.Val1068=
XM_011522480.1:c.2895G=	XP_011520782.1:p.Val965=
XM_011522481.1:c.2895G=	XP_011520783.1:p.Val965=
XR_932836.1:n.3472G=
XR_932837.1:n.3473G=
XR_932838.1:n.3473G=
NM_001351800.1:c.2895G=	NP_001338729.1:p.Val965=
NR_147784.1:n.3099G=
XM_011522479.2:c.3204G=	XP_011520781.1:p.Val1068=
XM_011522481.3:c.2895G=	XP_011520783.1:p.Val965=
XM_017023212.1:c.3069G=	XP_016878701.1:p.Val1023=
XM_017023214.1:c.3237G=	XP_016878703.1:p.Val1079=
XM_024450261.1:c.3273G=	XP_024306029.1:p.Val1091=
XR_932836.2:n.3418G=
XR_932837.3:n.3418G=
XR_932838.3:n.3418G=
NM_001171.6:c.3237G= MANE Select	NP_001162.5:p.Val1079=