Canonical Allele Identifier: CA2160140114

Gene: EXOC3L4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100526A= , CM000676.2:g.103100526A=	GRCh38
NC_000014.8:g.103566863A= , CM000676.1:g.103566863A=	GRCh37
NC_000014.7:g.102636616A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.307A=	ENSP00000508483.1:p.Thr103=
ENST00000688303.1:c.307A= MANE Select	ENSP00000509130.1:p.Thr103=
ENST00000380069.7:c.307A=	ENSP00000369409.3:p.Thr103=
ENST00000559116.1:c.199A=	ENSP00000454163.1:p.Thr67=
NM_001077594.1:c.307A=	NP_001071062.1:p.Thr103=
XM_011537323.1:c.481A=	XP_011535625.1:p.Thr161=
XM_011537324.1:c.481A=	XP_011535626.1:p.Thr161=
XM_011537325.1:c.307A=	XP_011535627.1:p.Thr103=
XM_011537326.1:c.307A=	XP_011535628.1:p.Thr103=
XM_011537327.1:c.307A=	XP_011535629.1:p.Thr103=
XM_011537328.1:c.307A=	XP_011535630.1:p.Thr103=
XM_011537329.1:c.307A=	XP_011535631.1:p.Thr103=
XM_011537330.1:c.307A=	XP_011535632.1:p.Thr103=
XM_011537331.1:c.307A=	XP_011535633.1:p.Thr103=
XM_011537332.1:c.307A=	XP_011535634.1:p.Thr103=
XM_011537333.1:c.418A=	XP_011535635.1:p.Thr140=
XM_011537334.1:c.-969A=	XP_011535636.1:n.-969A=
XR_943558.1:n.1036A=
XM_011537323.3:c.481A=	XP_011535625.1:p.Thr161=
XM_011537324.2:c.481A=	XP_011535626.1:p.Thr161=
XM_011537325.2:c.307A=	XP_011535627.1:p.Thr103=
XM_011537327.2:c.307A=	XP_011535629.1:p.Thr103=
XM_011537328.2:c.307A=	XP_011535630.1:p.Thr103=
XM_011537329.2:c.307A=	XP_011535631.1:p.Thr103=
XM_011537330.2:c.307A=	XP_011535632.1:p.Thr103=
XM_011537332.2:c.307A=	XP_011535634.1:p.Thr103=
XM_011537333.2:c.418A=	XP_011535635.1:p.Thr140=
XR_943558.2:n.1063A=
NM_001077594.2:c.307A= MANE Select	NP_001071062.1:p.Thr103=
NM_001394941.1:c.307A=	NP_001381870.1:p.Thr103=
NM_001394942.1:c.307A=	NP_001381871.1:p.Thr103=