Canonical Allele Identifier: CA1406089787
Gene: CLSTN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140456562A= , CM000665.2:g.140456562A= GRCh38
NC_000003.11:g.140175404A= , CM000665.1:g.140175404A= GRCh37
NC_000003.10:g.141658094A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458420.7:c.974-2959A= MANE Select ENSP00000402460.2:n.974-2959A=
ENST00000511524.1:n.1162-2959A=
ENST00000620185.1:c.782-2959A= ENSP00000478883.1:n.782-2959A=
NM_022131.2:c.974-2959A= NP_071414.2:n.974-2959A=
XR_924548.1:n.49-1809T=
XR_924549.1:n.49-1809T=
XM_017007022.2:c.899-2959A= XP_016862511.1:n.899-2959A=
XR_924548.2:n.1503-1809T=
XR_924549.2:n.1503-1809T=
NM_022131.3:c.974-2959A= MANE Select NP_071414.2:n.974-2959A=
Search 100 bp 5'
Search 100 bp 3'