Canonical Allele Identifier: CA899761541
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1264725827

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140528192A>G , CM000665.2:g.140528192A>G GRCh38
NC_000003.11:g.140247034A>G , CM000665.1:g.140247034A>G GRCh37
NC_000003.10:g.141729724A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458420.7:c.1345-4132A>G MANE Select ENSP00000402460.2:n.1345-4132A>G
ENST00000511524.1:n.1533-4132A>G
ENST00000620185.1:c.1153-4132A>G ENSP00000478883.1:n.1153-4132A>G
NM_022131.2:c.1345-4132A>G NP_071414.2:n.1345-4132A>G
XM_017007022.2:c.1270-4132A>G XP_016862511.1:n.1270-4132A>G
NM_022131.3:c.1345-4132A>G MANE Select NP_071414.2:n.1345-4132A>G