Canonical Allele Identifier: CA495129048

Gene: ABCC11

Linked Data

• MyVariant Identifiers: chr16:g.48258316T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48224405T>C , CM000678.2:g.48224405T>C	GRCh38
NC_000016.9:g.48258316T>C , CM000678.1:g.48258316T>C	GRCh37
NC_000016.8:g.46815817T>C	NCBI36
NG_011522.1:g.15773A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356608.7:c.420A>G MANE Select	ENSP00000349017.2:p.Glu140=
ENST00000353782.9:c.420A>G	ENSP00000311326.6:p.Glu140=
ENST00000356608.6:c.420A>G	ENSP00000349017.2:p.Glu140=
ENST00000394747.5:c.420A>G	ENSP00000378230.1:p.Glu140=
ENST00000394748.5:c.420A>G	ENSP00000378231.1:p.Glu140=
ENST00000567385.5:n.818A>G
ENST00000569991.1:c.420A>G	ENSP00000456268.1:p.Glu140=
NM_032583.3:c.420A>G	NP_115972.2:p.Glu140=
NM_033151.3:c.420A>G	NP_149163.2:p.Glu140=
NM_145186.2:c.420A>G	NP_660187.1:p.Glu140=
XM_011523396.1:c.222A>G	XP_011521698.1:p.Glu74=
XM_017023795.2:c.420A>G	XP_016879284.1:p.Glu140=
XM_017023796.2:c.420A>G	XP_016879285.1:p.Glu140=
XM_017023797.2:c.420A>G	XP_016879286.1:p.Glu140=
XM_017023798.2:c.420A>G	XP_016879287.1:p.Glu140=
XM_017023799.2:c.420A>G	XP_016879288.1:p.Glu140=
XM_017023800.2:c.420A>G	XP_016879289.1:p.Glu140=
XM_017023801.2:c.420A>G	XP_016879290.1:p.Glu140=
XM_017023803.1:c.420A>G	XP_016879292.1:p.Glu140=
XR_001752012.1:n.3098A>G
NM_001370496.1:c.420A>G	NP_001357425.1:p.Glu140=
NM_001370497.1:c.420A>G MANE Select	NP_001357426.1:p.Glu140=
NM_032583.4:c.420A>G	NP_115972.2:p.Glu140=
NM_033151.4:c.420A>G	NP_149163.2:p.Glu140=
NM_145186.3:c.420A>G	NP_660187.1:p.Glu140=