Canonical Allele Identifier: CA2949562

Gene: ODAM

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.70202789G>A , CM000666.2:g.70202789G>A	GRCh38
NC_000004.11:g.71068506G>A , CM000666.1:g.71068506G>A	GRCh37
NC_000004.10:g.71103095G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017855.4:c.682G>A MANE Select	NP_060325.3:p.Glu228Lys
ENST00000683306.1:c.682G>A MANE Select	ENSP00000507531.1:p.Glu228Lys
NM_001385579.1:c.634G>A	NP_001372508.1:p.Glu212Lys
NM_017855.3:c.682G>A	NP_060325.3:p.Glu228Lys
ENST00000396094.6:c.682G>A	ENSP00000379401.2:p.Glu228Lys
ENST00000510709.6:c.640G>A	ENSP00000423070.2:p.Glu214Lys
ENST00000510847.1:c.391G>A	ENSP00000422100.1:n.391G>A
ENST00000514097.5:c.493G>A	ENSP00000426106.1:p.Glu165Lys
XM_005265698.2:c.733G>A	XP_005265755.1:p.Glu245Lys
XM_005265698.3:c.733G>A	XP_005265755.1:p.Glu245Lys
XM_006714245.2:c.685G>A	XP_006714308.1:p.Glu229Lys
XM_006714245.4:c.685G>A	XP_006714308.1:p.Glu229Lys
XM_011532052.1:c.691G>A	XP_011530354.1:p.Glu231Lys
XM_017008331.1:c.640G>A	XP_016863820.1:p.Glu214Lys