Canonical Allele Identifier: CA391693570

Gene: EIF2AK4

Linked Data

• MyVariant Identifiers: chr15:g.40293315C>G (hg19) ; chr15:g.40001114C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40001114C>G , CM000677.2:g.40001114C>G	GRCh38
NC_000015.9:g.40293315C>G , CM000677.1:g.40293315C>G	GRCh37
NC_000015.8:g.38080607C>G	NCBI36
NG_034053.1:g.71991C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.3049C>G MANE Select	ENSP00000263791.5:p.His1017Asp
ENST00000263791.9:c.3049C>G	ENSP00000263791.5:p.His1017Asp
ENST00000558629.5:n.1966C>G
ENST00000560855.5:c.2381C>G
NM_001013703.3:c.3049C>G	NP_001013725.2:p.His1017Asp
XM_005254392.1:c.3049C>G	XP_005254449.1:p.His1017Asp
XM_011521599.1:c.3049C>G	XP_011519901.1:p.His1017Asp
XM_011521600.1:c.3049C>G	XP_011519902.1:p.His1017Asp
XM_005254392.3:c.3049C>G	XP_005254449.1:p.His1017Asp
XM_011521599.2:c.3049C>G	XP_011519901.1:p.His1017Asp
XM_011521600.3:c.3049C>G	XP_011519902.1:p.His1017Asp
XM_017022219.2:c.3049C>G	XP_016877708.1:p.His1017Asp
NM_001013703.4:c.3049C>G MANE Select	NP_001013725.2:p.His1017Asp