Canonical Allele Identifier: CA2220652567

Gene: ABCC11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48167600G= , CM000678.2:g.48167600G=	GRCh38
NC_000016.9:g.48201511G= , CM000678.1:g.48201511G=	GRCh37
NC_000016.8:g.46759012G=	NCBI36
NG_011522.1:g.72578C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356608.7:c.3952C= MANE Select	ENSP00000349017.2:p.Arg1318=
ENST00000353782.9:c.3838C=	ENSP00000311326.6:p.Arg1280=
ENST00000356608.6:c.3952C=	ENSP00000349017.2:p.Arg1318=
ENST00000394747.5:c.3952C=	ENSP00000378230.1:p.Arg1318=
ENST00000394748.5:c.3952C=	ENSP00000378231.1:p.Arg1318=
ENST00000565329.1:n.1252C=
NM_032583.3:c.3952C=	NP_115972.2:p.Arg1318=
NM_033151.3:c.3952C=	NP_149163.2:p.Arg1318=
NM_145186.2:c.3838C=	NP_660187.1:p.Arg1280=
XM_011523396.1:c.3754C=	XP_011521698.1:p.Arg1252=
XM_011523397.1:c.2995C=	XP_011521699.1:p.Arg999=
XM_011523398.1:c.2083C=	XP_011521700.1:p.Arg695=
XM_011523397.2:c.2995C=	XP_011521699.1:p.Arg999=
XM_011523398.3:c.2083C=	XP_011521700.1:p.Arg695=
XM_017023795.2:c.3952C=	XP_016879284.1:p.Arg1318=
XM_017023796.2:c.3952C=	XP_016879285.1:p.Arg1318=
XM_017023797.2:c.3952C=	XP_016879286.1:p.Arg1318=
XM_017023798.2:c.3952C=	XP_016879287.1:p.Arg1318=
XM_017023799.2:c.3952C=	XP_016879288.1:p.Arg1318=
XM_017023800.2:c.3952C=	XP_016879289.1:p.Arg1318=
XM_017023801.2:c.3844C=	XP_016879290.1:p.Arg1282=
XM_017023802.2:c.2995C=	XP_016879291.1:p.Arg999=
XM_024450475.1:c.2995C=	XP_024306243.1:p.Arg999=
XR_001752012.1:n.6630C=
NM_001370496.1:c.3958C=	NP_001357425.1:p.Arg1320=
NM_001370497.1:c.3952C= MANE Select	NP_001357426.1:p.Arg1318=
NM_032583.4:c.3952C=	NP_115972.2:p.Arg1318=
NM_033151.4:c.3952C=	NP_149163.2:p.Arg1318=
NM_145186.3:c.3838C=	NP_660187.1:p.Arg1280=