Canonical Allele Identifier: CA7759173

Gene: CERS3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100501691T>C , CM000677.2:g.100501691T>C	GRCh38
NC_000015.9:g.101041896T>C , CM000677.1:g.101041896T>C	GRCh37
NC_000015.8:g.98859419T>C	NCBI36
NG_042826.1:g.48030A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679737.1:c.159A>G MANE Select	ENSP00000506641.1:p.Arg53=
ENST00000284382.8:c.159A>G	ENSP00000284382.4:p.Arg53=
ENST00000394113.5:c.159A>G	ENSP00000377672.3:p.Arg53=
ENST00000538112.6:c.159A>G	ENSP00000437640.2:p.Arg53=
ENST00000558884.6:c.159A>G	ENSP00000453816.2:p.Arg53=
ENST00000559023.5:n.703A>G
ENST00000560944.1:n.93+43212A>G
NM_001290341.1:c.192A>G	NP_001277270.1:p.Arg64=
NM_001290341.2:c.192A>G	NP_001277270.1:p.Arg64=
NM_001290342.1:c.159A>G	NP_001277271.1:p.Arg53=
NM_001290342.2:c.159A>G	NP_001277271.1:p.Arg53=
NM_001290343.1:c.159A>G	NP_001277272.1:p.Arg53=
NM_178842.3:c.159A>G	NP_849164.2:p.Arg53=
NM_178842.4:c.159A>G	NP_849164.2:p.Arg53=
XM_011521355.1:c.192A>G	XP_011519657.1:p.Arg64=
XM_011521356.1:c.192A>G	XP_011519658.1:p.Arg64=
XM_011521357.1:c.192A>G	XP_011519659.1:p.Arg64=
XM_011521358.1:c.192A>G	XP_011519660.1:p.Arg64=
XM_011521355.2:c.192A>G	XP_011519657.1:p.Arg64=
XM_011521357.2:c.192A>G	XP_011519659.1:p.Arg64=
XM_017022002.1:c.192A>G	XP_016877491.1:p.Arg64=
XM_017022003.1:c.159A>G	XP_016877492.1:p.Arg53=
XM_017022004.1:c.159A>G	XP_016877493.1:p.Arg53=
NM_001290343.2:c.159A>G	NP_001277272.1:p.Arg53=
NM_178842.5:c.159A>G	NP_849164.2:p.Arg53=
NM_001378789.1:c.159A>G MANE Select	NP_001365718.1:p.Arg53=