Canonical Allele Identifier: CA7361855
Gene: EXOC3L4 HGNC NCBI

Linked Data

dbSNP Id: rs371303611

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.103100544G>T , CM000676.2:g.103100544G>T GRCh38
NC_000014.8:g.103566881G>T , CM000676.1:g.103566881G>T GRCh37
NC_000014.7:g.102636634G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000687959.1:c.325G>T ENSP00000508483.1:p.Gly109Trp
ENST00000688303.1:c.325G>T MANE Select ENSP00000509130.1:p.Gly109Trp
ENST00000380069.7:c.325G>T ENSP00000369409.3:p.Gly109Trp
ENST00000559116.1:c.217G>T ENSP00000454163.1:p.Gly73Trp
NM_001077594.1:c.325G>T NP_001071062.1:p.Gly109Trp
XM_011537323.1:c.499G>T XP_011535625.1:p.Gly167Trp
XM_011537324.1:c.499G>T XP_011535626.1:p.Gly167Trp
XM_011537325.1:c.325G>T XP_011535627.1:p.Gly109Trp
XM_011537326.1:c.325G>T XP_011535628.1:p.Gly109Trp
XM_011537327.1:c.325G>T XP_011535629.1:p.Gly109Trp
XM_011537328.1:c.325G>T XP_011535630.1:p.Gly109Trp
XM_011537329.1:c.325G>T XP_011535631.1:p.Gly109Trp
XM_011537330.1:c.325G>T XP_011535632.1:p.Gly109Trp
XM_011537331.1:c.325G>T XP_011535633.1:p.Gly109Trp
XM_011537332.1:c.325G>T XP_011535634.1:p.Gly109Trp
XM_011537333.1:c.436G>T XP_011535635.1:p.Gly146Trp
XM_011537334.1:c.-951G>T XP_011535636.1:n.-951G>T
XR_943558.1:n.1054G>T
XM_011537323.3:c.499G>T XP_011535625.1:p.Gly167Trp
XM_011537324.2:c.499G>T XP_011535626.1:p.Gly167Trp
XM_011537325.2:c.325G>T XP_011535627.1:p.Gly109Trp
XM_011537327.2:c.325G>T XP_011535629.1:p.Gly109Trp
XM_011537328.2:c.325G>T XP_011535630.1:p.Gly109Trp
XM_011537329.2:c.325G>T XP_011535631.1:p.Gly109Trp
XM_011537330.2:c.325G>T XP_011535632.1:p.Gly109Trp
XM_011537332.2:c.325G>T XP_011535634.1:p.Gly109Trp
XM_011537333.2:c.436G>T XP_011535635.1:p.Gly146Trp
XR_943558.2:n.1081G>T
NM_001077594.2:c.325G>T MANE Select NP_001071062.1:p.Gly109Trp
NM_001394941.1:c.325G>T NP_001381870.1:p.Gly109Trp
NM_001394942.1:c.325G>T NP_001381871.1:p.Gly109Trp