Canonical Allele Identifier: CA2141400756
Gene: HIF1A HGNC NCBI

Linked Data

dbSNP Id: rs946636053

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.61699958C>A , CM000676.2:g.61699958C>A GRCh38
NC_000014.8:g.62166676C>A , CM000676.1:g.62166676C>A GRCh37
NC_000014.7:g.61236429C>A NCBI36
NG_029606.1:g.9558C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337138.9:c.35+4119C>A MANE Select ENSP00000338018.4:n.35+4119C>A
ENST00000323441.10:c.35+4119C>A ENSP00000323326.6:n.35+4119C>A
ENST00000337138.8:c.35+4119C>A ENSP00000338018.4:n.35+4119C>A
ENST00000394997.5:c.35+4119C>A ENSP00000378446.1:n.35+4119C>A
ENST00000539097.2:c.104+2004C>A ENSP00000437955.1:n.104+2004C>A
ENST00000553999.5:n.327+4119C>A
ENST00000557206.1:n.52+1012C>A
ENST00000557446.5:n.327+4119C>A
ENST00000557538.5:c.-146+2004C>A ENSP00000451696.1:n.-146+2004C>A
NM_001243084.1:c.104+2004C>A NP_001230013.1:n.104+2004C>A
NM_001530.3:c.35+4119C>A NP_001521.1:n.35+4119C>A
NM_181054.2:c.35+4119C>A NP_851397.1:n.35+4119C>A
NM_001530.4:c.35+4119C>A MANE Select NP_001521.1:n.35+4119C>A
NM_181054.3:c.35+4119C>A NP_851397.1:n.35+4119C>A
NM_001243084.2:c.104+2004C>A NP_001230013.1:n.104+2004C>A