Canonical Allele Identifier: CA1406122937
Gene: CLSTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140528219C= , CM000665.2:g.140528219C= GRCh38
NC_000003.11:g.140247061C= , CM000665.1:g.140247061C= GRCh37
NC_000003.10:g.141729751C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458420.7:c.1345-4105C= MANE Select ENSP00000402460.2:n.1345-4105C=
ENST00000511524.1:n.1533-4105C=
ENST00000620185.1:c.1153-4105C= ENSP00000478883.1:n.1153-4105C=
NM_022131.2:c.1345-4105C= NP_071414.2:n.1345-4105C=
XM_017007022.2:c.1270-4105C= XP_016862511.1:n.1270-4105C=
NM_022131.3:c.1345-4105C= MANE Select NP_071414.2:n.1345-4105C=