Canonical Allele Identifier: CA2160140128

Gene: EXOC3L4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100551T= , CM000676.2:g.103100551T=	GRCh38
NC_000014.8:g.103566888T= , CM000676.1:g.103566888T=	GRCh37
NC_000014.7:g.102636641T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.332T=	ENSP00000508483.1:p.Met111=
ENST00000688303.1:c.332T= MANE Select	ENSP00000509130.1:p.Met111=
ENST00000380069.7:c.332T=	ENSP00000369409.3:p.Met111=
ENST00000559116.1:c.224T=	ENSP00000454163.1:p.Met75=
NM_001077594.1:c.332T=	NP_001071062.1:p.Met111=
XM_011537323.1:c.506T=	XP_011535625.1:p.Met169=
XM_011537324.1:c.506T=	XP_011535626.1:p.Met169=
XM_011537325.1:c.332T=	XP_011535627.1:p.Met111=
XM_011537326.1:c.332T=	XP_011535628.1:p.Met111=
XM_011537327.1:c.332T=	XP_011535629.1:p.Met111=
XM_011537328.1:c.332T=	XP_011535630.1:p.Met111=
XM_011537329.1:c.332T=	XP_011535631.1:p.Met111=
XM_011537330.1:c.332T=	XP_011535632.1:p.Met111=
XM_011537331.1:c.332T=	XP_011535633.1:p.Met111=
XM_011537332.1:c.332T=	XP_011535634.1:p.Met111=
XM_011537333.1:c.443T=	XP_011535635.1:p.Met148=
XM_011537334.1:c.-944T=	XP_011535636.1:n.-944T=
XR_943558.1:n.1061T=
XM_011537323.3:c.506T=	XP_011535625.1:p.Met169=
XM_011537324.2:c.506T=	XP_011535626.1:p.Met169=
XM_011537325.2:c.332T=	XP_011535627.1:p.Met111=
XM_011537327.2:c.332T=	XP_011535629.1:p.Met111=
XM_011537328.2:c.332T=	XP_011535630.1:p.Met111=
XM_011537329.2:c.332T=	XP_011535631.1:p.Met111=
XM_011537330.2:c.332T=	XP_011535632.1:p.Met111=
XM_011537332.2:c.332T=	XP_011535634.1:p.Met111=
XM_011537333.2:c.443T=	XP_011535635.1:p.Met148=
XR_943558.2:n.1088T=
NM_001077594.2:c.332T= MANE Select	NP_001071062.1:p.Met111=
NM_001394941.1:c.332T=	NP_001381870.1:p.Met111=
NM_001394942.1:c.332T=	NP_001381871.1:p.Met111=