Canonical Allele Identifier: CA1406122972
Gene: CLSTN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140528253A= , CM000665.2:g.140528253A= GRCh38
NC_000003.11:g.140247095A= , CM000665.1:g.140247095A= GRCh37
NC_000003.10:g.141729785A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458420.7:c.1345-4071A= MANE Select ENSP00000402460.2:n.1345-4071A=
ENST00000511524.1:n.1533-4071A=
ENST00000620185.1:c.1153-4071A= ENSP00000478883.1:n.1153-4071A=
NM_022131.2:c.1345-4071A= NP_071414.2:n.1345-4071A=
XM_017007022.2:c.1270-4071A= XP_016862511.1:n.1270-4071A=
NM_022131.3:c.1345-4071A= MANE Select NP_071414.2:n.1345-4071A=
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