Canonical Allele Identifier: CA347591917
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575166C>A , CM000664.2:g.88575166C>A GRCh38
NC_000002.11:g.88874684C>A , CM000664.1:g.88874684C>A GRCh37
NC_000002.10:g.88655799C>A NCBI36
NG_016424.1:g.57411G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2145G>T
ENST00000682276.1:n.1762G>T
ENST00000682892.1:c.1864G>T ENSP00000507214.1:p.Asp622Tyr
ENST00000682952.1:n.1956G>T
ENST00000684455.1:c.1530G>T
ENST00000684642.1:c.1714G>T ENSP00000507355.1:p.Asp572Tyr
ENST00000684740.1:n.2495G>T
ENST00000303236.9:c.2317G>T MANE Select ENSP00000307235.3:p.Asp773Tyr
ENST00000652099.1:c.2511G>T
ENST00000652736.1:n.2193G>T
ENST00000303236.7:c.2317G>T ENSP00000307235.3:p.Asp773Tyr
ENST00000415570.1:c.1954G>T ENSP00000412076.1:p.Asp652Tyr
ENST00000419748.5:c.1864G>T ENSP00000408325.1:p.Asp622Tyr
ENST00000470706.1:n.49-89G>T
NM_001313915.1:c.1864G>T NP_001300844.1:p.Asp622Tyr
NM_004836.5:c.2317G>T NP_004827.4:p.Asp773Tyr
NM_004836.6:c.2317G>T NP_004827.4:p.Asp773Tyr
NR_110236.1:n.1303C>A
XM_005264649.3:c.1633G>T XP_005264706.1:p.Asp545Tyr
XM_017005376.2:c.1633G>T XP_016860865.1:p.Asp545Tyr
NM_004836.7:c.2317G>T MANE Select NP_004827.4:p.Asp773Tyr
NM_001313915.2:c.1864G>T NP_001300844.1:p.Asp622Tyr