Canonical Allele Identifier: CA2210131871

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159514G= , CM000678.2:g.16159514G=	GRCh38
NC_000016.9:g.16253371G= , CM000678.1:g.16253371G=	GRCh37
NC_000016.8:g.16160872G=	NCBI36
NG_007558.2:g.68958C=
NG_007558.3:g.69104C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.3703C= MANE Select	NP_001162.5:p.Arg1235=
ENST00000205557.12:c.3703C= MANE Select	ENSP00000205557.7:p.Arg1235=
NM_001171.5:c.3703C=	NP_001162.4:p.Arg1235=
NM_001351800.1:c.3361C=	NP_001338729.1:p.Arg1121=
NR_147784.1:n.3365C=
ENST00000205557.11:c.3703C=	ENSP00000205557.7:p.Arg1235=
ENST00000456970.6:c.3328C=	ENSP00000405002.2:n.3328C=
ENST00000622290.4:c.*912C=	ENSP00000483331.1:n.*912C=
ENST00000622290.5:c.3703C=	ENSP00000483331.2:p.Arg1235=
ENST00000640696.1:c.517C=	ENSP00000492197.1:p.Arg173=
XM_011522479.1:c.3670C=	XP_011520781.1:p.Arg1224=
XM_011522479.2:c.3670C=	XP_011520781.1:p.Arg1224=
XM_011522480.1:c.3361C=	XP_011520782.1:p.Arg1121=
XM_011522481.1:c.3361C=	XP_011520783.1:p.Arg1121=
XM_011522481.3:c.3361C=	XP_011520783.1:p.Arg1121=
XM_017023212.1:c.3535C=	XP_016878701.1:p.Arg1179=
XM_024450261.1:c.3739C=	XP_024306029.1:p.Arg1247=
XR_932836.1:n.3938C=
XR_932836.2:n.3884C=
XR_932837.1:n.3739C=
XR_932837.3:n.3684C=
XR_932838.1:n.3739C=
XR_932838.3:n.3684C=
XR_933134.1:n.539-267G=