Canonical Allele Identifier: CA514469526

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35386822C>G , CM000684.2:g.35386822C>G	GRCh38
NC_000022.10:g.35782815C>G , CM000684.1:g.35782815C>G	GRCh37
NC_000022.9:g.34112815C>G	NCBI36
NG_023030.1:g.10756C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216117.9:c.282C>G MANE Select	ENSP00000216117.8:p.Ala94=
ENST00000481190.2:c.*187C>G	ENSP00000503987.1:n.*187C>G
ENST00000677931.1:c.145-3042C>G	ENSP00000502849.1:n.145-3042C>G
ENST00000678411.1:c.43-154C>G	ENSP00000503526.1:n.43-154C>G
ENST00000679074.1:c.282C>G	ENSP00000503459.1:p.Ala94=
ENST00000216117.8:c.282C>G	ENSP00000216117.8:p.Ala94=
ENST00000412893.5:c.282C>G	ENSP00000413316.1:p.Ala94=
ENST00000481190.1:n.496C>G
NM_002133.2:c.282C>G	NP_002124.1:p.Ala94=
NM_002133.3:c.282C>G MANE Select	NP_002124.1:p.Ala94=