Canonical Allele Identifier: CA2210152356

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198033G= , CM000678.2:g.16198033G=	GRCh38
NC_000016.9:g.16291890G= , CM000678.1:g.16291890G=	GRCh37
NC_000016.8:g.16199391G=	NCBI36
NG_007558.2:g.30439C=
NG_007558.3:g.30585C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1326C=	ENSP00000507301.1:p.Val442=
ENST00000622290.5:c.1326C=	ENSP00000483331.2:p.Val442=
ENST00000205557.12:c.1326C= MANE Select	ENSP00000205557.7:p.Val442=
ENST00000205557.11:c.1326C=	ENSP00000205557.7:p.Val442=
ENST00000456970.6:c.1326C=	ENSP00000405002.2:p.Val442=
ENST00000574094.5:n.1422C=
ENST00000622290.4:c.1326C=	ENSP00000483331.1:p.Val442=
NM_001171.5:c.1326C=	NP_001162.4:p.Val442=
XM_011522479.1:c.1326C=	XP_011520781.1:p.Val442=
XM_011522480.1:c.984C=	XP_011520782.1:p.Val328=
XM_011522481.1:c.984C=	XP_011520783.1:p.Val328=
XM_011522482.1:c.1326C=	XP_011520784.1:p.Val442=
XR_932836.1:n.1561C=
XR_932837.1:n.1562C=
XR_932838.1:n.1562C=
NM_001351800.1:c.984C=	NP_001338729.1:p.Val328=
NR_147784.1:n.1363C=
XM_011522479.2:c.1326C=	XP_011520781.1:p.Val442=
XM_011522481.3:c.984C=	XP_011520783.1:p.Val328=
XM_011522482.3:c.1326C=	XP_011520784.1:p.Val442=
XM_017023212.1:c.1326C=	XP_016878701.1:p.Val442=
XM_017023214.1:c.1326C=	XP_016878703.1:p.Val442=
XM_024450261.1:c.1362C=	XP_024306029.1:p.Val454=
XR_932836.2:n.1507C=
XR_932837.3:n.1507C=
XR_932838.3:n.1507C=
NM_001171.6:c.1326C= MANE Select	NP_001162.5:p.Val442=