Canonical Allele Identifier: CA2160140236

Gene: EXOC3L4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100738_103100742delinsATTCT , CM000676.2:g.103100738_103100742delinsATTCT	GRCh38
NC_000014.8:g.103567075_103567079delinsATTCT , CM000676.1:g.103567075_103567079delinsATTCT	GRCh37
NC_000014.7:g.102636828_102636832delinsATTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.394+125_394+129delinsATTCT	ENSP00000508483.1:n.394+125_394+129delinsATTCT
ENST00000688303.1:c.394+125_394+129delinsATTCT MANE Select	ENSP00000509130.1:n.394+125_394+129delinsATTCT
ENST00000380069.7:c.394+125_394+129delinsATTCT	ENSP00000369409.3:n.394+125_394+129delinsATTCT
ENST00000559116.1:c.286+125_286+129delinsATTCT	ENSP00000454163.1:n.286+125_286+129delinsATTCT
NM_001077594.1:c.394+125_394+129delinsATTCT	NP_001071062.1:n.394+125_394+129delinsATTCT
XM_011537323.1:c.568+125_568+129delinsATTCT	XP_011535625.1:n.568+125_568+129delinsATTCT
XM_011537324.1:c.568+125_568+129delinsATTCT	XP_011535626.1:n.568+125_568+129delinsATTCT
XM_011537325.1:c.394+125_394+129delinsATTCT	XP_011535627.1:n.394+125_394+129delinsATTCT
XM_011537326.1:c.394+125_394+129delinsATTCT	XP_011535628.1:n.394+125_394+129delinsATTCT
XM_011537327.1:c.394+125_394+129delinsATTCT	XP_011535629.1:n.394+125_394+129delinsATTCT
XM_011537328.1:c.394+125_394+129delinsATTCT	XP_011535630.1:n.394+125_394+129delinsATTCT
XM_011537329.1:c.394+125_394+129delinsATTCT	XP_011535631.1:n.394+125_394+129delinsATTCT
XM_011537330.1:c.394+125_394+129delinsATTCT	XP_011535632.1:n.394+125_394+129delinsATTCT
XM_011537331.1:c.394+125_394+129delinsATTCT	XP_011535633.1:n.394+125_394+129delinsATTCT
XM_011537332.1:c.394+125_394+129delinsATTCT	XP_011535634.1:n.394+125_394+129delinsATTCT
XM_011537333.1:c.505+125_505+129delinsATTCT	XP_011535635.1:n.505+125_505+129delinsATTCT
XM_011537334.1:c.-882+125_-882+129delinsATTCT	XP_011535636.1:n.-882+125_-882+129delinsATTCT
XR_943558.1:n.1123+125_1123+129delinsATTCT
XM_011537323.3:c.568+125_568+129delinsATTCT	XP_011535625.1:n.568+125_568+129delinsATTCT
XM_011537324.2:c.568+125_568+129delinsATTCT	XP_011535626.1:n.568+125_568+129delinsATTCT
XM_011537325.2:c.394+125_394+129delinsATTCT	XP_011535627.1:n.394+125_394+129delinsATTCT
XM_011537327.2:c.394+125_394+129delinsATTCT	XP_011535629.1:n.394+125_394+129delinsATTCT
XM_011537328.2:c.394+125_394+129delinsATTCT	XP_011535630.1:n.394+125_394+129delinsATTCT
XM_011537329.2:c.394+125_394+129delinsATTCT	XP_011535631.1:n.394+125_394+129delinsATTCT
XM_011537330.2:c.394+125_394+129delinsATTCT	XP_011535632.1:n.394+125_394+129delinsATTCT
XM_011537332.2:c.394+125_394+129delinsATTCT	XP_011535634.1:n.394+125_394+129delinsATTCT
XM_011537333.2:c.505+125_505+129delinsATTCT	XP_011535635.1:n.505+125_505+129delinsATTCT
XR_943558.2:n.1150+125_1150+129delinsATTCT
NM_001077594.2:c.394+125_394+129delinsATTCT MANE Select	NP_001071062.1:n.394+125_394+129delinsATTCT
NM_001394941.1:c.394+125_394+129delinsATTCT	NP_001381870.1:n.394+125_394+129delinsATTCT
NM_001394942.1:c.394+125_394+129delinsATTCT	NP_001381871.1:n.394+125_394+129delinsATTCT