Canonical Allele Identifier: CA2220652573

Gene: ABCC11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48167603G= , CM000678.2:g.48167603G=	GRCh38
NC_000016.9:g.48201514G= , CM000678.1:g.48201514G=	GRCh37
NC_000016.8:g.46759015G=	NCBI36
NG_011522.1:g.72575C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356608.7:c.3949C= MANE Select	ENSP00000349017.2:p.Gln1317=
ENST00000353782.9:c.3835C=	ENSP00000311326.6:p.Gln1279=
ENST00000356608.6:c.3949C=	ENSP00000349017.2:p.Gln1317=
ENST00000394747.5:c.3949C=	ENSP00000378230.1:p.Gln1317=
ENST00000394748.5:c.3949C=	ENSP00000378231.1:p.Gln1317=
ENST00000565329.1:n.1249C=
NM_032583.3:c.3949C=	NP_115972.2:p.Gln1317=
NM_033151.3:c.3949C=	NP_149163.2:p.Gln1317=
NM_145186.2:c.3835C=	NP_660187.1:p.Gln1279=
XM_011523396.1:c.3751C=	XP_011521698.1:p.Gln1251=
XM_011523397.1:c.2992C=	XP_011521699.1:p.Gln998=
XM_011523398.1:c.2080C=	XP_011521700.1:p.Gln694=
XM_011523397.2:c.2992C=	XP_011521699.1:p.Gln998=
XM_011523398.3:c.2080C=	XP_011521700.1:p.Gln694=
XM_017023795.2:c.3949C=	XP_016879284.1:p.Gln1317=
XM_017023796.2:c.3949C=	XP_016879285.1:p.Gln1317=
XM_017023797.2:c.3949C=	XP_016879286.1:p.Gln1317=
XM_017023798.2:c.3949C=	XP_016879287.1:p.Gln1317=
XM_017023799.2:c.3949C=	XP_016879288.1:p.Gln1317=
XM_017023800.2:c.3949C=	XP_016879289.1:p.Gln1317=
XM_017023801.2:c.3841C=	XP_016879290.1:p.Gln1281=
XM_017023802.2:c.2992C=	XP_016879291.1:p.Gln998=
XM_024450475.1:c.2992C=	XP_024306243.1:p.Gln998=
XR_001752012.1:n.6627C=
NM_001370496.1:c.3955C=	NP_001357425.1:p.Gln1319=
NM_001370497.1:c.3949C= MANE Select	NP_001357426.1:p.Gln1317=
NM_032583.4:c.3949C=	NP_115972.2:p.Gln1317=
NM_033151.4:c.3949C=	NP_149163.2:p.Gln1317=
NM_145186.3:c.3835C=	NP_660187.1:p.Gln1279=