Canonical Allele Identifier: CA1406089765
Gene: CLSTN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140456519C= , CM000665.2:g.140456519C= GRCh38
NC_000003.11:g.140175361C= , CM000665.1:g.140175361C= GRCh37
NC_000003.10:g.141658051C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458420.7:c.974-3002C= MANE Select ENSP00000402460.2:n.974-3002C=
ENST00000511524.1:n.1162-3002C=
ENST00000620185.1:c.782-3002C= ENSP00000478883.1:n.782-3002C=
NM_022131.2:c.974-3002C= NP_071414.2:n.974-3002C=
XR_924548.1:n.49-1766G=
XR_924549.1:n.49-1766G=
XM_017007022.2:c.899-3002C= XP_016862511.1:n.899-3002C=
XR_924548.2:n.1503-1766G=
XR_924549.2:n.1503-1766G=
NM_022131.3:c.974-3002C= MANE Select NP_071414.2:n.974-3002C=
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