Canonical Allele Identifier: CA514469222

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35387002C>T , CM000684.2:g.35387002C>T	GRCh38
NC_000022.10:g.35782995C>T , CM000684.1:g.35782995C>T	GRCh37
NC_000022.9:g.34112995C>T	NCBI36
NG_023030.1:g.10936C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216117.9:c.462C>T MANE Select	ENSP00000216117.8:p.Ala154=
ENST00000481190.2:c.*367C>T	ENSP00000503987.1:n.*367C>T
ENST00000677931.1:c.145-2862C>T	ENSP00000502849.1:n.145-2862C>T
ENST00000678411.1:c.69C>T	ENSP00000503526.1:p.Ala23=
ENST00000679074.1:c.462C>T	ENSP00000503459.1:p.Ala154=
ENST00000216117.8:c.462C>T	ENSP00000216117.8:p.Ala154=
ENST00000412893.5:c.462C>T	ENSP00000413316.1:p.Ala154=
NM_002133.2:c.462C>T	NP_002124.1:p.Ala154=
NM_002133.3:c.462C>T MANE Select	NP_002124.1:p.Ala154=