Canonical Allele Identifier: CA2210133399

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149813C= , CM000678.2:g.16149813C=	GRCh38
NC_000016.9:g.16243670C= , CM000678.1:g.16243670C=	GRCh37
NC_000016.8:g.16151171C=	NCBI36
NG_007558.2:g.78659G=
NG_007558.3:g.78805G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*1004G=	ENSP00000483331.2:n.*1004G=
ENST00000205557.12:c.*320G= MANE Select	ENSP00000205557.7:n.*320G=
ENST00000640696.1:c.1646G=	ENSP00000492197.1:n.1646G=
ENST00000205557.11:c.*320G=	ENSP00000205557.7:n.*320G=
ENST00000576204.5:n.1695G=
ENST00000622290.4:c.*2041G=	ENSP00000483331.1:n.*2041G=
NM_001171.5:c.*320G=	NP_001162.4:n.*320G=
XM_011522479.1:c.*320G=	XP_011520781.1:n.*320G=
XM_011522480.1:c.*320G=	XP_011520782.1:n.*320G=
XM_011522481.1:c.*320G=	XP_011520783.1:n.*320G=
XR_933134.1:n.538+5523C=
NM_001351800.1:c.*320G=	NP_001338729.1:n.*320G=
NR_147784.1:n.4494G=
XM_011522479.2:c.*320G=	XP_011520781.1:n.*320G=
XM_011522481.3:c.*320G=	XP_011520783.1:n.*320G=
XM_017023212.1:c.*320G=	XP_016878701.1:n.*320G=
XM_024450261.1:c.*320G=	XP_024306029.1:n.*320G=
NM_001171.6:c.*320G= MANE Select	NP_001162.5:n.*320G=