Canonical Allele Identifier: CA1406122970

Gene: CLSTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140528252T= , CM000665.2:g.140528252T=	GRCh38
NC_000003.11:g.140247094T= , CM000665.1:g.140247094T=	GRCh37
NC_000003.10:g.141729784T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000458420.7:c.1345-4072T= MANE Select	ENSP00000402460.2:n.1345-4072T=
ENST00000511524.1:n.1533-4072T=
ENST00000620185.1:c.1153-4072T=	ENSP00000478883.1:n.1153-4072T=
NM_022131.2:c.1345-4072T=	NP_071414.2:n.1345-4072T=
XM_017007022.2:c.1270-4072T=	XP_016862511.1:n.1270-4072T=
NM_022131.3:c.1345-4072T= MANE Select	NP_071414.2:n.1345-4072T=