Canonical Allele Identifier: CA2210152591

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198142A= , CM000678.2:g.16198142A=	GRCh38
NC_000016.9:g.16291999A= , CM000678.1:g.16291999A=	GRCh37
NC_000016.8:g.16199500A=	NCBI36
NG_007558.2:g.30330T=
NG_007558.3:g.30476T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1217T=	ENSP00000507301.1:p.Val406=
ENST00000622290.5:c.1217T=	ENSP00000483331.2:p.Val406=
ENST00000205557.12:c.1217T= MANE Select	ENSP00000205557.7:p.Val406=
ENST00000205557.11:c.1217T=	ENSP00000205557.7:p.Val406=
ENST00000456970.6:c.1217T=	ENSP00000405002.2:p.Val406=
ENST00000574094.5:n.1313T=
ENST00000622290.4:c.1217T=	ENSP00000483331.1:p.Val406=
NM_001171.5:c.1217T=	NP_001162.4:p.Val406=
XM_011522479.1:c.1217T=	XP_011520781.1:p.Val406=
XM_011522480.1:c.875T=	XP_011520782.1:p.Val292=
XM_011522481.1:c.875T=	XP_011520783.1:p.Val292=
XM_011522482.1:c.1217T=	XP_011520784.1:p.Val406=
XR_932836.1:n.1452T=
XR_932837.1:n.1453T=
XR_932838.1:n.1453T=
NM_001351800.1:c.875T=	NP_001338729.1:p.Val292=
NR_147784.1:n.1254T=
XM_011522479.2:c.1217T=	XP_011520781.1:p.Val406=
XM_011522481.3:c.875T=	XP_011520783.1:p.Val292=
XM_011522482.3:c.1217T=	XP_011520784.1:p.Val406=
XM_017023212.1:c.1217T=	XP_016878701.1:p.Val406=
XM_017023214.1:c.1217T=	XP_016878703.1:p.Val406=
XM_024450261.1:c.1253T=	XP_024306029.1:p.Val418=
XR_932836.2:n.1398T=
XR_932837.3:n.1398T=
XR_932838.3:n.1398T=
NM_001171.6:c.1217T= MANE Select	NP_001162.5:p.Val406=