Canonical Allele Identifier: CA427173301
Gene: EIF2AK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.88874987G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575469G>T , CM000664.2:g.88575469G>T GRCh38
NC_000002.11:g.88874987G>T , CM000664.1:g.88874987G>T GRCh37
NC_000002.10:g.88656102G>T NCBI36
NG_016424.1:g.57108C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.1865-23C>A
ENST00000682276.1:n.1482-23C>A
ENST00000682892.1:c.1584-23C>A ENSP00000507214.1:n.1584-23C>A
ENST00000682952.1:n.1676-23C>A
ENST00000684455.1:c.1250-23C>A
ENST00000684642.1:c.1434-23C>A ENSP00000507355.1:n.1434-23C>A
ENST00000684740.1:n.2215-23C>A
ENST00000303236.9:c.2037-23C>A MANE Select ENSP00000307235.3:n.2037-23C>A
ENST00000652099.1:c.2231-23C>A
ENST00000652736.1:n.1913-23C>A
ENST00000303236.7:c.2037-23C>A ENSP00000307235.3:n.2037-23C>A
ENST00000415570.1:c.1674-23C>A ENSP00000412076.1:n.1674-23C>A
ENST00000419748.5:c.1584-23C>A ENSP00000408325.1:n.1584-23C>A
ENST00000478003.1:n.603-23C>A
NM_001313915.1:c.1584-23C>A NP_001300844.1:n.1584-23C>A
NM_004836.5:c.2037-23C>A NP_004827.4:n.2037-23C>A
NM_004836.6:c.2037-23C>A NP_004827.4:n.2037-23C>A
NR_110236.1:n.1606G>T
XM_005264649.3:c.1353-23C>A XP_005264706.1:n.1353-23C>A
XR_939749.1:n.2316-23C>A
XM_017005376.2:c.1353-23C>A XP_016860865.1:n.1353-23C>A
NM_004836.7:c.2037-23C>A MANE Select NP_004827.4:n.2037-23C>A
NM_001313915.2:c.1584-23C>A NP_001300844.1:n.1584-23C>A