Canonical Allele Identifier: CA2626692360

Gene: EXOC3L4

Linked Data

• gnomAD v4: 14-103100762-T-TGGAGACC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100762_103100763insGGAGACC , CM000676.2:g.103100762_103100763insGGAGACC	GRCh38
NC_000014.8:g.103567099_103567100insGGAGACC , CM000676.1:g.103567099_103567100insGGAGACC	GRCh37
NC_000014.7:g.102636852_102636853insGGAGACC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.394+149_394+150insGGAGACC	ENSP00000508483.1:n.394+149_394+150insGGAGACC
ENST00000688303.1:c.394+149_394+150insGGAGACC MANE Select	ENSP00000509130.1:n.394+149_394+150insGGAGACC
ENST00000380069.7:c.394+149_394+150insGGAGACC	ENSP00000369409.3:n.394+149_394+150insGGAGACC
ENST00000559116.1:c.286+149_286+150insGGAGACC	ENSP00000454163.1:n.286+149_286+150insGGAGACC
NM_001077594.1:c.394+149_394+150insGGAGACC	NP_001071062.1:n.394+149_394+150insGGAGACC
XM_011537323.1:c.568+149_568+150insGGAGACC	XP_011535625.1:n.568+149_568+150insGGAGACC
XM_011537324.1:c.568+149_568+150insGGAGACC	XP_011535626.1:n.568+149_568+150insGGAGACC
XM_011537325.1:c.394+149_394+150insGGAGACC	XP_011535627.1:n.394+149_394+150insGGAGACC
XM_011537326.1:c.394+149_394+150insGGAGACC	XP_011535628.1:n.394+149_394+150insGGAGACC
XM_011537327.1:c.394+149_394+150insGGAGACC	XP_011535629.1:n.394+149_394+150insGGAGACC
XM_011537328.1:c.394+149_394+150insGGAGACC	XP_011535630.1:n.394+149_394+150insGGAGACC
XM_011537329.1:c.394+149_394+150insGGAGACC	XP_011535631.1:n.394+149_394+150insGGAGACC
XM_011537330.1:c.394+149_394+150insGGAGACC	XP_011535632.1:n.394+149_394+150insGGAGACC
XM_011537331.1:c.394+149_394+150insGGAGACC	XP_011535633.1:n.394+149_394+150insGGAGACC
XM_011537332.1:c.394+149_394+150insGGAGACC	XP_011535634.1:n.394+149_394+150insGGAGACC
XM_011537333.1:c.505+149_505+150insGGAGACC	XP_011535635.1:n.505+149_505+150insGGAGACC
XM_011537334.1:c.-882+149_-882+150insGGAGACC	XP_011535636.1:n.-882+149_-882+150insGGAGACC
XR_943558.1:n.1123+149_1123+150insGGAGACC
XM_011537323.3:c.568+149_568+150insGGAGACC	XP_011535625.1:n.568+149_568+150insGGAGACC
XM_011537324.2:c.568+149_568+150insGGAGACC	XP_011535626.1:n.568+149_568+150insGGAGACC
XM_011537325.2:c.394+149_394+150insGGAGACC	XP_011535627.1:n.394+149_394+150insGGAGACC
XM_011537327.2:c.394+149_394+150insGGAGACC	XP_011535629.1:n.394+149_394+150insGGAGACC
XM_011537328.2:c.394+149_394+150insGGAGACC	XP_011535630.1:n.394+149_394+150insGGAGACC
XM_011537329.2:c.394+149_394+150insGGAGACC	XP_011535631.1:n.394+149_394+150insGGAGACC
XM_011537330.2:c.394+149_394+150insGGAGACC	XP_011535632.1:n.394+149_394+150insGGAGACC
XM_011537332.2:c.394+149_394+150insGGAGACC	XP_011535634.1:n.394+149_394+150insGGAGACC
XM_011537333.2:c.505+149_505+150insGGAGACC	XP_011535635.1:n.505+149_505+150insGGAGACC
XR_943558.2:n.1150+149_1150+150insGGAGACC
NM_001077594.2:c.394+149_394+150insGGAGACC MANE Select	NP_001071062.1:n.394+149_394+150insGGAGACC
NM_001394941.1:c.394+149_394+150insGGAGACC	NP_001381870.1:n.394+149_394+150insGGAGACC
NM_001394942.1:c.394+149_394+150insGGAGACC	NP_001381871.1:n.394+149_394+150insGGAGACC