Canonical Allele Identifier: CA2210134167

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150240C= , CM000678.2:g.16150240C=	GRCh38
NC_000016.9:g.16244097C= , CM000678.1:g.16244097C=	GRCh37
NC_000016.8:g.16151598C=	NCBI36
NG_007558.2:g.78232G=
NG_007558.3:g.78378G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*577G=	ENSP00000483331.2:n.*577G=
ENST00000205557.12:c.4405G= MANE Select	ENSP00000205557.7:p.Val1469=
ENST00000640696.1:c.1219G=	ENSP00000492197.1:p.Val407=
ENST00000205557.11:c.4405G=	ENSP00000205557.7:p.Val1469=
ENST00000456970.6:c.4030G=	ENSP00000405002.2:n.4030G=
ENST00000576204.5:n.1268G=
ENST00000622290.4:c.*1614G=	ENSP00000483331.1:n.*1614G=
NM_001171.5:c.4405G=	NP_001162.4:p.Val1469=
XM_011522479.1:c.4372G=	XP_011520781.1:p.Val1458=
XM_011522480.1:c.4063G=	XP_011520782.1:p.Val1355=
XM_011522481.1:c.4063G=	XP_011520783.1:p.Val1355=
XR_933134.1:n.538+5950C=
NM_001351800.1:c.4063G=	NP_001338729.1:p.Val1355=
NR_147784.1:n.4067G=
XM_011522479.2:c.4372G=	XP_011520781.1:p.Val1458=
XM_011522481.3:c.4063G=	XP_011520783.1:p.Val1355=
XM_017023212.1:c.4237G=	XP_016878701.1:p.Val1413=
XM_024450261.1:c.4441G=	XP_024306029.1:p.Val1481=
NM_001171.6:c.4405G= MANE Select	NP_001162.5:p.Val1469=