Canonical Allele Identifier: CA411352551

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35386900G>T , CM000684.2:g.35386900G>T	GRCh38
NC_000022.10:g.35782893G>T , CM000684.1:g.35782893G>T	GRCh37
NC_000022.9:g.34112893G>T	NCBI36
NG_023030.1:g.10834G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002133.3:c.360G>T MANE Select	NP_002124.1:p.Glu120Asp
ENST00000216117.9:c.360G>T MANE Select	ENSP00000216117.8:p.Glu120Asp
NM_002133.2:c.360G>T	NP_002124.1:p.Glu120Asp
ENST00000216117.8:c.360G>T	ENSP00000216117.8:p.Glu120Asp
ENST00000412893.5:c.360G>T	ENSP00000413316.1:p.Glu120Asp
ENST00000481190.1:n.574G>T
ENST00000481190.2:c.*265G>T	ENSP00000503987.1:n.*265G>T
ENST00000677931.1:c.145-2964G>T	ENSP00000502849.1:n.145-2964G>T
ENST00000678411.1:c.43-76G>T	ENSP00000503526.1:n.43-76G>T
ENST00000679074.1:c.360G>T	ENSP00000503459.1:p.Glu120Asp