Canonical Allele Identifier: CA617218450

Gene: EIF2AK4

Linked Data

• dbSNP Id: rs1465263033
• gnomAD v2: 15-40270326-AG-A
• gnomAD v4: 15-39978125-AG-A
• MyVariant Identifiers: chr15:g.40270327del (hg19) ; chr15:g.39978126del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39978126del , CM000677.2:g.39978126del	GRCh38
NC_000015.9:g.40270327del , CM000677.1:g.40270327del	GRCh37
NC_000015.8:g.38057619del	NCBI36
NG_034053.1:g.49003del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.2298del MANE Select	ENSP00000263791.5:p.Asn767ThrfsTer24
ENST00000263791.9:c.2298del	ENSP00000263791.5:p.Asn767ThrfsTer24
ENST00000560855.5:c.1714del
ENST00000624709.1:n.1148del
NM_001013703.3:c.2298del	NP_001013725.2:p.Asn767ThrfsTer24
XM_005254392.1:c.2298del	XP_005254449.1:p.Asn767ThrfsTer24
XM_011521599.1:c.2298del	XP_011519901.1:p.Asn767ThrfsTer24
XM_011521600.1:c.2298del	XP_011519902.1:p.Asn767ThrfsTer24
XM_005254392.3:c.2298del	XP_005254449.1:p.Asn767ThrfsTer24
XM_011521599.2:c.2298del	XP_011519901.1:p.Asn767ThrfsTer24
XM_011521600.3:c.2298del	XP_011519902.1:p.Asn767ThrfsTer24
XM_017022219.2:c.2298del	XP_016877708.1:p.Asn767ThrfsTer24
NM_001013703.4:c.2298del MANE Select	NP_001013725.2:p.Asn767ThrfsTer24