Canonical Allele Identifier: CA2160140091

Gene: EXOC3L4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100486A= , CM000676.2:g.103100486A=	GRCh38
NC_000014.8:g.103566823A= , CM000676.1:g.103566823A=	GRCh37
NC_000014.7:g.102636576A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.267A=	ENSP00000508483.1:p.Gln89=
ENST00000688303.1:c.267A= MANE Select	ENSP00000509130.1:p.Gln89=
ENST00000380069.7:c.267A=	ENSP00000369409.3:p.Gln89=
ENST00000559116.1:c.159A=	ENSP00000454163.1:p.Gln53=
NM_001077594.1:c.267A=	NP_001071062.1:p.Gln89=
XM_011537323.1:c.441A=	XP_011535625.1:p.Gln147=
XM_011537324.1:c.441A=	XP_011535626.1:p.Gln147=
XM_011537325.1:c.267A=	XP_011535627.1:p.Gln89=
XM_011537326.1:c.267A=	XP_011535628.1:p.Gln89=
XM_011537327.1:c.267A=	XP_011535629.1:p.Gln89=
XM_011537328.1:c.267A=	XP_011535630.1:p.Gln89=
XM_011537329.1:c.267A=	XP_011535631.1:p.Gln89=
XM_011537330.1:c.267A=	XP_011535632.1:p.Gln89=
XM_011537331.1:c.267A=	XP_011535633.1:p.Gln89=
XM_011537332.1:c.267A=	XP_011535634.1:p.Gln89=
XM_011537333.1:c.378A=	XP_011535635.1:p.Gln126=
XR_943558.1:n.996A=
XM_011537323.3:c.441A=	XP_011535625.1:p.Gln147=
XM_011537324.2:c.441A=	XP_011535626.1:p.Gln147=
XM_011537325.2:c.267A=	XP_011535627.1:p.Gln89=
XM_011537327.2:c.267A=	XP_011535629.1:p.Gln89=
XM_011537328.2:c.267A=	XP_011535630.1:p.Gln89=
XM_011537329.2:c.267A=	XP_011535631.1:p.Gln89=
XM_011537330.2:c.267A=	XP_011535632.1:p.Gln89=
XM_011537332.2:c.267A=	XP_011535634.1:p.Gln89=
XM_011537333.2:c.378A=	XP_011535635.1:p.Gln126=
XR_943558.2:n.1023A=
NM_001077594.2:c.267A= MANE Select	NP_001071062.1:p.Gln89=
NM_001394941.1:c.267A=	NP_001381870.1:p.Gln89=
NM_001394942.1:c.267A=	NP_001381871.1:p.Gln89=