Canonical Allele Identifier: CA10204728

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35386992C>T , CM000684.2:g.35386992C>T	GRCh38
NC_000022.10:g.35782985C>T , CM000684.1:g.35782985C>T	GRCh37
NC_000022.9:g.34112985C>T	NCBI36
NG_023030.1:g.10926C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216117.9:c.452C>T MANE Select	ENSP00000216117.8:p.Ala151Val
ENST00000481190.2:c.*357C>T	ENSP00000503987.1:n.*357C>T
ENST00000677931.1:c.145-2872C>T	ENSP00000502849.1:n.145-2872C>T
ENST00000678411.1:c.59C>T	ENSP00000503526.1:p.Ala20Val
ENST00000679074.1:c.452C>T	ENSP00000503459.1:p.Ala151Val
ENST00000216117.8:c.452C>T	ENSP00000216117.8:p.Ala151Val
ENST00000412893.5:c.452C>T	ENSP00000413316.1:p.Ala151Val
NM_002133.2:c.452C>T	NP_002124.1:p.Ala151Val
NM_002133.3:c.452C>T MANE Select	NP_002124.1:p.Ala151Val