Canonical Allele Identifier: CA1406122809
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1935179457

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140528042A>T , CM000665.2:g.140528042A>T GRCh38
NC_000003.11:g.140246884A>T , CM000665.1:g.140246884A>T GRCh37
NC_000003.10:g.141729574A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458420.7:c.1345-4282A>T MANE Select ENSP00000402460.2:n.1345-4282A>T
ENST00000511524.1:n.1533-4282A>T
ENST00000620185.1:c.1153-4282A>T ENSP00000478883.1:n.1153-4282A>T
NM_022131.2:c.1345-4282A>T NP_071414.2:n.1345-4282A>T
XM_017007022.2:c.1270-4282A>T XP_016862511.1:n.1270-4282A>T
NM_022131.3:c.1345-4282A>T MANE Select NP_071414.2:n.1345-4282A>T