Canonical Allele Identifier: CA2210143335

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169841C= , CM000678.2:g.16169841C=	GRCh38
NC_000016.9:g.16263698C= , CM000678.1:g.16263698C=	GRCh37
NC_000016.8:g.16171199C=	NCBI36
NG_007558.2:g.58631G=
NG_007558.3:g.58777G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2800G=	ENSP00000483331.2:p.Val934=
ENST00000205557.12:c.2800G= MANE Select	ENSP00000205557.7:p.Val934=
ENST00000205557.11:c.2800G=	ENSP00000205557.7:p.Val934=
ENST00000456970.6:c.2625G=	ENSP00000405002.2:n.2625G=
ENST00000622290.4:c.*9G=	ENSP00000483331.1:n.*9G=
NM_001171.5:c.2800G=	NP_001162.4:p.Val934=
XM_011522479.1:c.2767G=	XP_011520781.1:p.Val923=
XM_011522480.1:c.2458G=	XP_011520782.1:p.Val820=
XM_011522481.1:c.2458G=	XP_011520783.1:p.Val820=
XR_932836.1:n.3035G=
XR_932837.1:n.3036G=
XR_932838.1:n.3036G=
NM_001351800.1:c.2458G=	NP_001338729.1:p.Val820=
NR_147784.1:n.2662G=
XM_011522479.2:c.2767G=	XP_011520781.1:p.Val923=
XM_011522481.3:c.2458G=	XP_011520783.1:p.Val820=
XM_017023212.1:c.2632G=	XP_016878701.1:p.Val878=
XM_017023214.1:c.2800G=	XP_016878703.1:p.Val934=
XM_024450261.1:c.2836G=	XP_024306029.1:p.Val946=
XR_932836.2:n.2981G=
XR_932837.3:n.2981G=
XR_932838.3:n.2981G=
NM_001171.6:c.2800G= MANE Select	NP_001162.5:p.Val934=