Canonical Allele Identifier: CA2949251

Gene: ODAM

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.70196591C>A , CM000666.2:g.70196591C>A	GRCh38
NC_000004.11:g.71062308C>A , CM000666.1:g.71062308C>A	GRCh37
NC_000004.10:g.71096897C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017855.4:c.48C>A MANE Select	NP_060325.3:p.Ala16=
ENST00000683306.1:c.48C>A MANE Select	ENSP00000507531.1:p.Ala16=
NM_001385579.1:c.48C>A	NP_001372508.1:p.Ala16=
NM_017855.3:c.48C>A	NP_060325.3:p.Ala16=
ENST00000396094.6:c.48C>A	ENSP00000379401.2:p.Ala16=
ENST00000510709.6:c.48C>A	ENSP00000423070.2:p.Ala16=
XM_005265698.2:c.99C>A	XP_005265755.1:p.Ala33=
XM_005265698.3:c.99C>A	XP_005265755.1:p.Ala33=
XM_006714245.2:c.99C>A	XP_006714308.1:p.Ala33=
XM_006714245.4:c.99C>A	XP_006714308.1:p.Ala33=
XM_011532052.1:c.99C>A	XP_011530354.1:p.Ala33=
XM_017008331.1:c.48C>A	XP_016863820.1:p.Ala16=