Canonical Allele Identifier: CA1406089780

Gene: CLSTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140456551C= , CM000665.2:g.140456551C=	GRCh38
NC_000003.11:g.140175393C= , CM000665.1:g.140175393C=	GRCh37
NC_000003.10:g.141658083C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000458420.7:c.974-2970C= MANE Select	ENSP00000402460.2:n.974-2970C=
ENST00000511524.1:n.1162-2970C=
ENST00000620185.1:c.782-2970C=	ENSP00000478883.1:n.782-2970C=
NM_022131.2:c.974-2970C=	NP_071414.2:n.974-2970C=
XR_924548.1:n.49-1798G=
XR_924549.1:n.49-1798G=
XM_017007022.2:c.899-2970C=	XP_016862511.1:n.899-2970C=
XR_924548.2:n.1503-1798G=
XR_924549.2:n.1503-1798G=
NM_022131.3:c.974-2970C= MANE Select	NP_071414.2:n.974-2970C=