Canonical Allele Identifier: CA2510878207

Gene: HIF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61700003_61700004insG , CM000676.2:g.61700003_61700004insG	GRCh38
NC_000014.8:g.62166721_62166722insG , CM000676.1:g.62166721_62166722insG	GRCh37
NC_000014.7:g.61236474_61236475insG	NCBI36
NG_029606.1:g.9603_9604insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337138.9:c.35+4164_35+4165insG MANE Select	ENSP00000338018.4:n.35+4164_35+4165insG
ENST00000323441.10:c.35+4164_35+4165insG	ENSP00000323326.6:n.35+4164_35+4165insG
ENST00000337138.8:c.35+4164_35+4165insG	ENSP00000338018.4:n.35+4164_35+4165insG
ENST00000394997.5:c.35+4164_35+4165insG	ENSP00000378446.1:n.35+4164_35+4165insG
ENST00000539097.2:c.104+2049_104+2050insG	ENSP00000437955.1:n.104+2049_104+2050insG
ENST00000553999.5:n.327+4164_327+4165insG
ENST00000557206.1:n.52+1057_52+1058insG
ENST00000557446.5:n.327+4164_327+4165insG
ENST00000557538.5:c.-146+2049_-146+2050insG	ENSP00000451696.1:n.-146+2049_-146+2050insG
NM_001243084.1:c.104+2049_104+2050insG	NP_001230013.1:n.104+2049_104+2050insG
NM_001530.3:c.35+4164_35+4165insG	NP_001521.1:n.35+4164_35+4165insG
NM_181054.2:c.35+4164_35+4165insG	NP_851397.1:n.35+4164_35+4165insG
NM_001530.4:c.35+4164_35+4165insG MANE Select	NP_001521.1:n.35+4164_35+4165insG
NM_181054.3:c.35+4164_35+4165insG	NP_851397.1:n.35+4164_35+4165insG
NM_001243084.2:c.104+2049_104+2050insG	NP_001230013.1:n.104+2049_104+2050insG