Canonical Allele Identifier: CA347801
Gene: CSTB HGNC NCBI

Linked Data

ClinVar Variation Id: 161420
ClinVar RCV Id: RCV000202562
dbSNP Id: rs312262707

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43774642_43774659del , CM000683.2:g.43774642_43774659del GRCh38
NC_000021.8:g.45194523_45194540del , CM000683.1:g.45194523_45194540del GRCh37
NC_000021.7:g.44018951_44018968del NCBI36
NG_011545.1:g.6723_6740del , LRG_485:g.6723_6740del

Transcript Alleles

HGVS Amino-acid change
ENST00000291568.7:c.168+2_168+19del
ENST00000480147.3:n.1613_1630del
ENST00000639959.1:c.36-326_36-309del
ENST00000640406.1:c.170_187del ENSP00000492672.1:p.Val57_Gln62del
ENST00000675996.1:n.593+2_593+19del
ENST00000291568.5:c.168+2_168+19del
ENST00000480147.1:n.207_224del
NM_000100.3:c.168+2_168+19del , LRG_485t1:c.168+2_168+19del
NM_000100.4:c.168+2_168+19del