Canonical Allele Identifier: CA2210140611

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154767G= , CM000678.2:g.16154767G=	GRCh38
NC_000016.9:g.16248624G= , CM000678.1:g.16248624G=	GRCh37
NC_000016.8:g.16156125G=	NCBI36
NG_007558.2:g.73705C=
NG_007558.3:g.73851C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.4069C= MANE Select	NP_001162.5:p.Arg1357=
ENST00000205557.12:c.4069C= MANE Select	ENSP00000205557.7:p.Arg1357=
NM_001171.5:c.4069C=	NP_001162.4:p.Arg1357=
NM_001351800.1:c.3727C=	NP_001338729.1:p.Arg1243=
NR_147784.1:n.3731C=
ENST00000205557.11:c.4069C=	ENSP00000205557.7:p.Arg1357=
ENST00000456970.6:c.3694C=	ENSP00000405002.2:n.3694C=
ENST00000576204.5:n.932C=
ENST00000576204.6:n.932C=
ENST00000622290.4:c.*1278C=	ENSP00000483331.1:n.*1278C=
ENST00000622290.5:c.*241C=	ENSP00000483331.2:n.*241C=
ENST00000640696.1:c.883C=	ENSP00000492197.1:p.Arg295=
XM_011522479.1:c.4036C=	XP_011520781.1:p.Arg1346=
XM_011522479.2:c.4036C=	XP_011520781.1:p.Arg1346=
XM_011522480.1:c.3727C=	XP_011520782.1:p.Arg1243=
XM_011522481.1:c.3727C=	XP_011520783.1:p.Arg1243=
XM_011522481.3:c.3727C=	XP_011520783.1:p.Arg1243=
XM_017023212.1:c.3901C=	XP_016878701.1:p.Arg1301=
XM_024450261.1:c.4105C=	XP_024306029.1:p.Arg1369=
XR_933134.1:n.539-5014G=