Canonical Allele Identifier: CA2171566142

Gene: EIF2AK4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39977962_39977963delinsTG , CM000677.2:g.39977962_39977963delinsTG	GRCh38
NC_000015.9:g.40270163_40270164delinsTG , CM000677.1:g.40270163_40270164delinsTG	GRCh37
NC_000015.8:g.38057455_38057456delinsTG	NCBI36
NG_034053.1:g.48839_48840delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.2250-116_2250-115delinsTG MANE Select	ENSP00000263791.5:n.2250-116_2250-115delinsTG
ENST00000263791.9:c.2250-116_2250-115delinsTG	ENSP00000263791.5:n.2250-116_2250-115delinsTG
ENST00000560855.5:c.1666-116_1666-115delinsTG
ENST00000624709.1:n.984_985delinsTG
NM_001013703.3:c.2250-116_2250-115delinsTG	NP_001013725.2:n.2250-116_2250-115delinsTG
XM_005254392.1:c.2250-116_2250-115delinsTG	XP_005254449.1:n.2250-116_2250-115delinsTG
XM_011521599.1:c.2250-116_2250-115delinsTG	XP_011519901.1:n.2250-116_2250-115delinsTG
XM_011521600.1:c.2250-116_2250-115delinsTG	XP_011519902.1:n.2250-116_2250-115delinsTG
XM_005254392.3:c.2250-116_2250-115delinsTG	XP_005254449.1:n.2250-116_2250-115delinsTG
XM_011521599.2:c.2250-116_2250-115delinsTG	XP_011519901.1:n.2250-116_2250-115delinsTG
XM_011521600.3:c.2250-116_2250-115delinsTG	XP_011519902.1:n.2250-116_2250-115delinsTG
XM_017022219.2:c.2250-116_2250-115delinsTG	XP_016877708.1:n.2250-116_2250-115delinsTG
NM_001013703.4:c.2250-116_2250-115delinsTG MANE Select	NP_001013725.2:n.2250-116_2250-115delinsTG