Canonical Allele Identifier: CA2581883754

Gene: EIF4E3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.71746592C= , CM000665.2:g.71746592C=	GRCh38
NC_000003.11:g.71795743C= , CM000665.1:g.71795743C=	GRCh37
NC_000003.10:g.71878433C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647725.1:c.-959+7623G=	ENSP00000497585.1:n.-959+7623G=
ENST00000295612.7:c.-291+6871G=	ENSP00000295612.3:n.-291+6871G=
ENST00000421769.6:c.-291+8052G=	ENSP00000411762.2:n.-291+8052G=
ENST00000448225.5:c.-291+7623G=	ENSP00000410350.1:n.-291+7623G=
ENST00000496214.6:c.-291+7623G=	ENSP00000417889.2:n.-291+7623G=
NM_001134649.2:c.-291+7623G=	NP_001128121.1:n.-291+7623G=
NM_001282886.1:c.-291+6871G=	NP_001269815.1:n.-291+6871G=
NM_173359.4:c.-291+8052G=	NP_775495.1:n.-291+8052G=
XM_017006282.2:c.-341+7623G=	XP_016861771.1:n.-341+7623G=
NM_001282886.2:c.-291+6871G=	NP_001269815.1:n.-291+6871G=
NM_173359.5:c.-291+8052G=	NP_775495.1:n.-291+8052G=
NM_001134649.3:c.-291+7623G=	NP_001128121.1:n.-291+7623G=