Canonical Allele Identifier: CA2210140914

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154917C= , CM000678.2:g.16154917C=	GRCh38
NC_000016.9:g.16248774C= , CM000678.1:g.16248774C=	GRCh37
NC_000016.8:g.16156275C=	NCBI36
NG_007558.2:g.73555G=
NG_007558.3:g.73701G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.860G=
ENST00000622290.5:c.*169G=	ENSP00000483331.2:n.*169G=
ENST00000205557.12:c.3997G= MANE Select	ENSP00000205557.7:p.Val1333=
ENST00000640696.1:c.811G=	ENSP00000492197.1:p.Val271=
ENST00000205557.11:c.3997G=	ENSP00000205557.7:p.Val1333=
ENST00000456970.6:c.3622G=	ENSP00000405002.2:n.3622G=
ENST00000576204.5:n.860G=
ENST00000622290.4:c.*1206G=	ENSP00000483331.1:n.*1206G=
NM_001171.5:c.3997G=	NP_001162.4:p.Val1333=
XM_011522479.1:c.3964G=	XP_011520781.1:p.Val1322=
XM_011522480.1:c.3655G=	XP_011520782.1:p.Val1219=
XM_011522481.1:c.3655G=	XP_011520783.1:p.Val1219=
XR_933134.1:n.539-4864C=
NM_001351800.1:c.3655G=	NP_001338729.1:p.Val1219=
NR_147784.1:n.3659G=
XM_011522479.2:c.3964G=	XP_011520781.1:p.Val1322=
XM_011522481.3:c.3655G=	XP_011520783.1:p.Val1219=
XM_017023212.1:c.3829G=	XP_016878701.1:p.Val1277=
XM_024450261.1:c.4033G=	XP_024306029.1:p.Val1345=
NM_001171.6:c.3997G= MANE Select	NP_001162.5:p.Val1333=