Canonical Allele Identifier: CA2626692335

Gene: EXOC3L4

Linked Data

• gnomAD v4: 14-103100741-C-CTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100744_103100745insTTTT , CM000676.2:g.103100744_103100745insTTTT	GRCh38
NC_000014.8:g.103567081_103567082insTTTT , CM000676.1:g.103567081_103567082insTTTT	GRCh37
NC_000014.7:g.102636834_102636835insTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.394+131_394+132insTTTT	ENSP00000508483.1:n.394+131_394+132insTTTT
ENST00000688303.1:c.394+131_394+132insTTTT MANE Select	ENSP00000509130.1:n.394+131_394+132insTTTT
ENST00000380069.7:c.394+131_394+132insTTTT	ENSP00000369409.3:n.394+131_394+132insTTTT
ENST00000559116.1:c.286+131_286+132insTTTT	ENSP00000454163.1:n.286+131_286+132insTTTT
NM_001077594.1:c.394+131_394+132insTTTT	NP_001071062.1:n.394+131_394+132insTTTT
XM_011537323.1:c.568+131_568+132insTTTT	XP_011535625.1:n.568+131_568+132insTTTT
XM_011537324.1:c.568+131_568+132insTTTT	XP_011535626.1:n.568+131_568+132insTTTT
XM_011537325.1:c.394+131_394+132insTTTT	XP_011535627.1:n.394+131_394+132insTTTT
XM_011537326.1:c.394+131_394+132insTTTT	XP_011535628.1:n.394+131_394+132insTTTT
XM_011537327.1:c.394+131_394+132insTTTT	XP_011535629.1:n.394+131_394+132insTTTT
XM_011537328.1:c.394+131_394+132insTTTT	XP_011535630.1:n.394+131_394+132insTTTT
XM_011537329.1:c.394+131_394+132insTTTT	XP_011535631.1:n.394+131_394+132insTTTT
XM_011537330.1:c.394+131_394+132insTTTT	XP_011535632.1:n.394+131_394+132insTTTT
XM_011537331.1:c.394+131_394+132insTTTT	XP_011535633.1:n.394+131_394+132insTTTT
XM_011537332.1:c.394+131_394+132insTTTT	XP_011535634.1:n.394+131_394+132insTTTT
XM_011537333.1:c.505+131_505+132insTTTT	XP_011535635.1:n.505+131_505+132insTTTT
XM_011537334.1:c.-882+131_-882+132insTTTT	XP_011535636.1:n.-882+131_-882+132insTTTT
XR_943558.1:n.1123+131_1123+132insTTTT
XM_011537323.3:c.568+131_568+132insTTTT	XP_011535625.1:n.568+131_568+132insTTTT
XM_011537324.2:c.568+131_568+132insTTTT	XP_011535626.1:n.568+131_568+132insTTTT
XM_011537325.2:c.394+131_394+132insTTTT	XP_011535627.1:n.394+131_394+132insTTTT
XM_011537327.2:c.394+131_394+132insTTTT	XP_011535629.1:n.394+131_394+132insTTTT
XM_011537328.2:c.394+131_394+132insTTTT	XP_011535630.1:n.394+131_394+132insTTTT
XM_011537329.2:c.394+131_394+132insTTTT	XP_011535631.1:n.394+131_394+132insTTTT
XM_011537330.2:c.394+131_394+132insTTTT	XP_011535632.1:n.394+131_394+132insTTTT
XM_011537332.2:c.394+131_394+132insTTTT	XP_011535634.1:n.394+131_394+132insTTTT
XM_011537333.2:c.505+131_505+132insTTTT	XP_011535635.1:n.505+131_505+132insTTTT
XR_943558.2:n.1150+131_1150+132insTTTT
NM_001077594.2:c.394+131_394+132insTTTT MANE Select	NP_001071062.1:n.394+131_394+132insTTTT
NM_001394941.1:c.394+131_394+132insTTTT	NP_001381870.1:n.394+131_394+132insTTTT
NM_001394942.1:c.394+131_394+132insTTTT	NP_001381871.1:n.394+131_394+132insTTTT