Canonical Allele Identifier: CA2626692350

Gene: EXOC3L4

Linked Data

• gnomAD v4: 14-103100757-C-CCCTGTCTCAAATAA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100757_103100758insCCTGTCTCAAATAA , CM000676.2:g.103100757_103100758insCCTGTCTCAAATAA	GRCh38
NC_000014.8:g.103567094_103567095insCCTGTCTCAAATAA , CM000676.1:g.103567094_103567095insCCTGTCTCAAATAA	GRCh37
NC_000014.7:g.102636847_102636848insCCTGTCTCAAATAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.394+144_394+145insCCTGTCTCAAATAA	ENSP00000508483.1:n.394+144_394+145insCCTGTCTCAAATAA
ENST00000688303.1:c.394+144_394+145insCCTGTCTCAAATAA MANE Select	ENSP00000509130.1:n.394+144_394+145insCCTGTCTCAAATAA
ENST00000380069.7:c.394+144_394+145insCCTGTCTCAAATAA	ENSP00000369409.3:n.394+144_394+145insCCTGTCTCAAATAA
ENST00000559116.1:c.286+144_286+145insCCTGTCTCAAATAA	ENSP00000454163.1:n.286+144_286+145insCCTGTCTCAAATAA
NM_001077594.1:c.394+144_394+145insCCTGTCTCAAATAA	NP_001071062.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537323.1:c.568+144_568+145insCCTGTCTCAAATAA	XP_011535625.1:n.568+144_568+145insCCTGTCTCAAATAA
XM_011537324.1:c.568+144_568+145insCCTGTCTCAAATAA	XP_011535626.1:n.568+144_568+145insCCTGTCTCAAATAA
XM_011537325.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535627.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537326.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535628.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537327.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535629.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537328.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535630.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537329.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535631.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537330.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535632.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537331.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535633.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537332.1:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535634.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537333.1:c.505+144_505+145insCCTGTCTCAAATAA	XP_011535635.1:n.505+144_505+145insCCTGTCTCAAATAA
XM_011537334.1:c.-882+144_-882+145insCCTGTCTCAAATAA	XP_011535636.1:n.-882+144_-882+145insCCTGTCTCAAATAA
XR_943558.1:n.1123+144_1123+145insCCTGTCTCAAATAA
XM_011537323.3:c.568+144_568+145insCCTGTCTCAAATAA	XP_011535625.1:n.568+144_568+145insCCTGTCTCAAATAA
XM_011537324.2:c.568+144_568+145insCCTGTCTCAAATAA	XP_011535626.1:n.568+144_568+145insCCTGTCTCAAATAA
XM_011537325.2:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535627.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537327.2:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535629.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537328.2:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535630.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537329.2:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535631.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537330.2:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535632.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537332.2:c.394+144_394+145insCCTGTCTCAAATAA	XP_011535634.1:n.394+144_394+145insCCTGTCTCAAATAA
XM_011537333.2:c.505+144_505+145insCCTGTCTCAAATAA	XP_011535635.1:n.505+144_505+145insCCTGTCTCAAATAA
XR_943558.2:n.1150+144_1150+145insCCTGTCTCAAATAA
NM_001077594.2:c.394+144_394+145insCCTGTCTCAAATAA MANE Select	NP_001071062.1:n.394+144_394+145insCCTGTCTCAAATAA
NM_001394941.1:c.394+144_394+145insCCTGTCTCAAATAA	NP_001381870.1:n.394+144_394+145insCCTGTCTCAAATAA
NM_001394942.1:c.394+144_394+145insCCTGTCTCAAATAA	NP_001381871.1:n.394+144_394+145insCCTGTCTCAAATAA