Canonical Allele Identifier: CA2220718414

Gene: ABCC11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48224349T= , CM000678.2:g.48224349T=	GRCh38
NC_000016.9:g.48258260T= , CM000678.1:g.48258260T=	GRCh37
NC_000016.8:g.46815761T=	NCBI36
NG_011522.1:g.15829A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356608.7:c.476A= MANE Select	ENSP00000349017.2:p.Gln159=
ENST00000353782.9:c.476A=	ENSP00000311326.6:p.Gln159=
ENST00000356608.6:c.476A=	ENSP00000349017.2:p.Gln159=
ENST00000394747.5:c.476A=	ENSP00000378230.1:p.Gln159=
ENST00000394748.5:c.476A=	ENSP00000378231.1:p.Gln159=
ENST00000567385.5:n.874A=
ENST00000569991.1:c.476A=	ENSP00000456268.1:p.Gln159=
NM_032583.3:c.476A=	NP_115972.2:p.Gln159=
NM_033151.3:c.476A=	NP_149163.2:p.Gln159=
NM_145186.2:c.476A=	NP_660187.1:p.Gln159=
XM_011523396.1:c.278A=	XP_011521698.1:p.Gln93=
XM_017023795.2:c.476A=	XP_016879284.1:p.Gln159=
XM_017023796.2:c.476A=	XP_016879285.1:p.Gln159=
XM_017023797.2:c.476A=	XP_016879286.1:p.Gln159=
XM_017023798.2:c.476A=	XP_016879287.1:p.Gln159=
XM_017023799.2:c.476A=	XP_016879288.1:p.Gln159=
XM_017023800.2:c.476A=	XP_016879289.1:p.Gln159=
XM_017023801.2:c.476A=	XP_016879290.1:p.Gln159=
XM_017023803.1:c.476A=	XP_016879292.1:p.Gln159=
XR_001752012.1:n.3154A=
NM_001370496.1:c.476A=	NP_001357425.1:p.Gln159=
NM_001370497.1:c.476A= MANE Select	NP_001357426.1:p.Gln159=
NM_032583.4:c.476A=	NP_115972.2:p.Gln159=
NM_033151.4:c.476A=	NP_149163.2:p.Gln159=
NM_145186.3:c.476A=	NP_660187.1:p.Gln159=