Canonical Allele Identifier: CA2160140239

Gene: EXOC3L4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103100741_103100745delinsCTTTA , CM000676.2:g.103100741_103100745delinsCTTTA	GRCh38
NC_000014.8:g.103567078_103567082delinsCTTTA , CM000676.1:g.103567078_103567082delinsCTTTA	GRCh37
NC_000014.7:g.102636831_102636835delinsCTTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687959.1:c.394+128_394+132delinsCTTTA	ENSP00000508483.1:n.394+128_394+132delinsCTTTA
ENST00000688303.1:c.394+128_394+132delinsCTTTA MANE Select	ENSP00000509130.1:n.394+128_394+132delinsCTTTA
ENST00000380069.7:c.394+128_394+132delinsCTTTA	ENSP00000369409.3:n.394+128_394+132delinsCTTTA
ENST00000559116.1:c.286+128_286+132delinsCTTTA	ENSP00000454163.1:n.286+128_286+132delinsCTTTA
NM_001077594.1:c.394+128_394+132delinsCTTTA	NP_001071062.1:n.394+128_394+132delinsCTTTA
XM_011537323.1:c.568+128_568+132delinsCTTTA	XP_011535625.1:n.568+128_568+132delinsCTTTA
XM_011537324.1:c.568+128_568+132delinsCTTTA	XP_011535626.1:n.568+128_568+132delinsCTTTA
XM_011537325.1:c.394+128_394+132delinsCTTTA	XP_011535627.1:n.394+128_394+132delinsCTTTA
XM_011537326.1:c.394+128_394+132delinsCTTTA	XP_011535628.1:n.394+128_394+132delinsCTTTA
XM_011537327.1:c.394+128_394+132delinsCTTTA	XP_011535629.1:n.394+128_394+132delinsCTTTA
XM_011537328.1:c.394+128_394+132delinsCTTTA	XP_011535630.1:n.394+128_394+132delinsCTTTA
XM_011537329.1:c.394+128_394+132delinsCTTTA	XP_011535631.1:n.394+128_394+132delinsCTTTA
XM_011537330.1:c.394+128_394+132delinsCTTTA	XP_011535632.1:n.394+128_394+132delinsCTTTA
XM_011537331.1:c.394+128_394+132delinsCTTTA	XP_011535633.1:n.394+128_394+132delinsCTTTA
XM_011537332.1:c.394+128_394+132delinsCTTTA	XP_011535634.1:n.394+128_394+132delinsCTTTA
XM_011537333.1:c.505+128_505+132delinsCTTTA	XP_011535635.1:n.505+128_505+132delinsCTTTA
XM_011537334.1:c.-882+128_-882+132delinsCTTTA	XP_011535636.1:n.-882+128_-882+132delinsCTTTA
XR_943558.1:n.1123+128_1123+132delinsCTTTA
XM_011537323.3:c.568+128_568+132delinsCTTTA	XP_011535625.1:n.568+128_568+132delinsCTTTA
XM_011537324.2:c.568+128_568+132delinsCTTTA	XP_011535626.1:n.568+128_568+132delinsCTTTA
XM_011537325.2:c.394+128_394+132delinsCTTTA	XP_011535627.1:n.394+128_394+132delinsCTTTA
XM_011537327.2:c.394+128_394+132delinsCTTTA	XP_011535629.1:n.394+128_394+132delinsCTTTA
XM_011537328.2:c.394+128_394+132delinsCTTTA	XP_011535630.1:n.394+128_394+132delinsCTTTA
XM_011537329.2:c.394+128_394+132delinsCTTTA	XP_011535631.1:n.394+128_394+132delinsCTTTA
XM_011537330.2:c.394+128_394+132delinsCTTTA	XP_011535632.1:n.394+128_394+132delinsCTTTA
XM_011537332.2:c.394+128_394+132delinsCTTTA	XP_011535634.1:n.394+128_394+132delinsCTTTA
XM_011537333.2:c.505+128_505+132delinsCTTTA	XP_011535635.1:n.505+128_505+132delinsCTTTA
XR_943558.2:n.1150+128_1150+132delinsCTTTA
NM_001077594.2:c.394+128_394+132delinsCTTTA MANE Select	NP_001071062.1:n.394+128_394+132delinsCTTTA
NM_001394941.1:c.394+128_394+132delinsCTTTA	NP_001381870.1:n.394+128_394+132delinsCTTTA
NM_001394942.1:c.394+128_394+132delinsCTTTA	NP_001381871.1:n.394+128_394+132delinsCTTTA