Canonical Allele Identifier: CA2171566088

Gene: EIF2AK4

Linked Data

• dbSNP Id: rs2034722536
• gnomAD v4: 15-39977842-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39977842C>T , CM000677.2:g.39977842C>T	GRCh38
NC_000015.9:g.40270043C>T , CM000677.1:g.40270043C>T	GRCh37
NC_000015.8:g.38057335C>T	NCBI36
NG_034053.1:g.48719C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.2250-236C>T MANE Select	ENSP00000263791.5:n.2250-236C>T
ENST00000263791.9:c.2250-236C>T	ENSP00000263791.5:n.2250-236C>T
ENST00000560855.5:c.1666-236C>T
ENST00000624709.1:n.864C>T
NM_001013703.3:c.2250-236C>T	NP_001013725.2:n.2250-236C>T
XM_005254392.1:c.2250-236C>T	XP_005254449.1:n.2250-236C>T
XM_011521599.1:c.2250-236C>T	XP_011519901.1:n.2250-236C>T
XM_011521600.1:c.2250-236C>T	XP_011519902.1:n.2250-236C>T
XM_005254392.3:c.2250-236C>T	XP_005254449.1:n.2250-236C>T
XM_011521599.2:c.2250-236C>T	XP_011519901.1:n.2250-236C>T
XM_011521600.3:c.2250-236C>T	XP_011519902.1:n.2250-236C>T
XM_017022219.2:c.2250-236C>T	XP_016877708.1:n.2250-236C>T
NM_001013703.4:c.2250-236C>T MANE Select	NP_001013725.2:n.2250-236C>T