Canonical Allele Identifier: CA2141400813
Gene: HIF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.61700061T= , CM000676.2:g.61700061T= GRCh38
NC_000014.8:g.62166779T= , CM000676.1:g.62166779T= GRCh37
NC_000014.7:g.61236532T= NCBI36
NG_029606.1:g.9661T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337138.9:c.35+4222T= MANE Select ENSP00000338018.4:n.35+4222T=
ENST00000323441.10:c.35+4222T= ENSP00000323326.6:n.35+4222T=
ENST00000337138.8:c.35+4222T= ENSP00000338018.4:n.35+4222T=
ENST00000394997.5:c.35+4222T= ENSP00000378446.1:n.35+4222T=
ENST00000539097.2:c.104+2107T= ENSP00000437955.1:n.104+2107T=
ENST00000553999.5:n.327+4222T=
ENST00000557206.1:n.52+1115T=
ENST00000557446.5:n.327+4222T=
ENST00000557538.5:c.-146+2107T= ENSP00000451696.1:n.-146+2107T=
NM_001243084.1:c.104+2107T= NP_001230013.1:n.104+2107T=
NM_001530.3:c.35+4222T= NP_001521.1:n.35+4222T=
NM_181054.2:c.35+4222T= NP_851397.1:n.35+4222T=
NM_001530.4:c.35+4222T= MANE Select NP_001521.1:n.35+4222T=
NM_181054.3:c.35+4222T= NP_851397.1:n.35+4222T=
NM_001243084.2:c.104+2107T= NP_001230013.1:n.104+2107T=