Canonical Allele Identifier: CA10204656

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35386744C>G , CM000684.2:g.35386744C>G	GRCh38
NC_000022.10:g.35782737C>G , CM000684.1:g.35782737C>G	GRCh37
NC_000022.9:g.34112737C>G	NCBI36
NG_023030.1:g.10678C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216117.9:c.204C>G MANE Select	ENSP00000216117.8:p.Asn68Lys
ENST00000481190.2:c.*109C>G	ENSP00000503987.1:n.*109C>G
ENST00000677931.1:c.145-3120C>G	ENSP00000502849.1:n.145-3120C>G
ENST00000678411.1:c.43-232C>G	ENSP00000503526.1:n.43-232C>G
ENST00000679074.1:c.204C>G	ENSP00000503459.1:p.Asn68Lys
ENST00000216117.8:c.204C>G	ENSP00000216117.8:p.Asn68Lys
ENST00000412893.5:c.204C>G	ENSP00000413316.1:p.Asn68Lys
ENST00000481190.1:n.418C>G
NM_002133.2:c.204C>G	NP_002124.1:p.Asn68Lys
NM_002133.3:c.204C>G MANE Select	NP_002124.1:p.Asn68Lys