Canonical Allele Identifier: CA1406122843

Gene: CLSTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140528140_140528143delinsGTCC , CM000665.2:g.140528140_140528143delinsGTCC	GRCh38
NC_000003.11:g.140246982_140246985delinsGTCC , CM000665.1:g.140246982_140246985delinsGTCC	GRCh37
NC_000003.10:g.141729672_141729675delinsGTCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458420.7:c.1345-4184_1345-4181delinsGTCC MANE Select	ENSP00000402460.2:n.1345-4184_1345-4181delinsGTCC
ENST00000511524.1:n.1533-4184_1533-4181delinsGTCC
ENST00000620185.1:c.1153-4184_1153-4181delinsGTCC	ENSP00000478883.1:n.1153-4184_1153-4181delinsGTCC
NM_022131.2:c.1345-4184_1345-4181delinsGTCC	NP_071414.2:n.1345-4184_1345-4181delinsGTCC
XM_017007022.2:c.1270-4184_1270-4181delinsGTCC	XP_016862511.1:n.1270-4184_1270-4181delinsGTCC
NM_022131.3:c.1345-4184_1345-4181delinsGTCC MANE Select	NP_071414.2:n.1345-4184_1345-4181delinsGTCC