Canonical Allele Identifier: CA2160139948
Gene: EXOC3L4 HGNC NCBI

Linked Data

dbSNP Id: rs1890091428

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.103100196G>A , CM000676.2:g.103100196G>A GRCh38
NC_000014.8:g.103566533G>A , CM000676.1:g.103566533G>A GRCh37
NC_000014.7:g.102636286G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000687959.1:c.-16-8G>A ENSP00000508483.1:n.-16-8G>A
ENST00000688303.1:c.-16-8G>A MANE Select ENSP00000509130.1:n.-16-8G>A
ENST00000380069.7:c.-24G>A ENSP00000369409.3:n.-24G>A
NM_001077594.1:c.-24G>A NP_001071062.1:n.-24G>A
XM_011537323.1:c.159-8G>A XP_011535625.1:n.159-8G>A
XM_011537324.1:c.159-8G>A XP_011535626.1:n.159-8G>A
XM_011537325.1:c.-16-8G>A XP_011535627.1:n.-16-8G>A
XM_011537326.1:c.-16-8G>A XP_011535628.1:n.-16-8G>A
XM_011537327.1:c.-16-8G>A XP_011535629.1:n.-16-8G>A
XM_011537328.1:c.-16-8G>A XP_011535630.1:n.-16-8G>A
XM_011537329.1:c.-16-8G>A XP_011535631.1:n.-16-8G>A
XM_011537330.1:c.-16-8G>A XP_011535632.1:n.-16-8G>A
XM_011537331.1:c.-16-8G>A XP_011535633.1:n.-16-8G>A
XM_011537332.1:c.-16-8G>A XP_011535634.1:n.-16-8G>A
XM_011537333.1:c.96-8G>A XP_011535635.1:n.96-8G>A
XR_943558.1:n.714-8G>A
XM_011537323.3:c.159-8G>A XP_011535625.1:n.159-8G>A
XM_011537324.2:c.159-8G>A XP_011535626.1:n.159-8G>A
XM_011537325.2:c.-16-8G>A XP_011535627.1:n.-16-8G>A
XM_011537327.2:c.-16-8G>A XP_011535629.1:n.-16-8G>A
XM_011537328.2:c.-16-8G>A XP_011535630.1:n.-16-8G>A
XM_011537329.2:c.-16-8G>A XP_011535631.1:n.-16-8G>A
XM_011537330.2:c.-16-8G>A XP_011535632.1:n.-16-8G>A
XM_011537332.2:c.-16-8G>A XP_011535634.1:n.-16-8G>A
XM_011537333.2:c.96-8G>A XP_011535635.1:n.96-8G>A
XR_943558.2:n.741-8G>A
NM_001077594.2:c.-16-8G>A MANE Select NP_001071062.1:n.-16-8G>A
NM_001394941.1:c.-16-8G>A NP_001381870.1:n.-16-8G>A
NM_001394942.1:c.-16-8G>A NP_001381871.1:n.-16-8G>A