Canonical Allele Identifier: CA2322142239

Gene: OLFM2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9857465C= , CM000681.2:g.9857465C=	GRCh38
NC_000019.9:g.9968141C= , CM000681.1:g.9968141C=	GRCh37
NC_000019.8:g.9829141C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_058164.4:c.378G= MANE Select	NP_477512.1:p.Met126=
ENST00000264833.9:c.378G= MANE Select	ENSP00000264833.3:p.Met126=
NM_001304347.1:c.450G=	NP_001291276.1:p.Met150=
NM_001304347.2:c.450G=	NP_001291276.1:p.Met150=
NM_001304348.1:c.144G=	NP_001291277.1:p.Met48=
NM_001304348.2:c.144G=	NP_001291277.1:p.Met48=
NM_058164.3:c.378G=	NP_477512.1:p.Met126=
ENST00000264833.8:c.378G=	ENSP00000264833.3:p.Met126=
ENST00000590410.1:n.336G=
ENST00000590841.5:c.144G=	ENSP00000464877.1:p.Met48=
ENST00000592448.1:c.144G=	ENSP00000466018.1:p.Met48=
ENST00000593091.1:c.450G=	ENSP00000465809.1:p.Met150=
ENST00000593091.2:c.450G=	ENSP00000465809.2:p.Met150=