Canonical Allele Identifier: CA10204675

Gene: HMOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35386801T>C , CM000684.2:g.35386801T>C	GRCh38
NC_000022.10:g.35782794T>C , CM000684.1:g.35782794T>C	GRCh37
NC_000022.9:g.34112794T>C	NCBI36
NG_023030.1:g.10735T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216117.9:c.261T>C MANE Select	ENSP00000216117.8:p.Ala87=
ENST00000481190.2:c.*166T>C	ENSP00000503987.1:n.*166T>C
ENST00000677931.1:c.145-3063T>C	ENSP00000502849.1:n.145-3063T>C
ENST00000678411.1:c.43-175T>C	ENSP00000503526.1:n.43-175T>C
ENST00000679074.1:c.261T>C	ENSP00000503459.1:p.Ala87=
ENST00000216117.8:c.261T>C	ENSP00000216117.8:p.Ala87=
ENST00000412893.5:c.261T>C	ENSP00000413316.1:p.Ala87=
ENST00000481190.1:n.475T>C
NM_002133.2:c.261T>C	NP_002124.1:p.Ala87=
NM_002133.3:c.261T>C MANE Select	NP_002124.1:p.Ala87=