Canonical Allele Identifier: CA30094935

Gene: CTSS

Linked Data

• dbSNP Id: rs367582792
• gnomAD v4: 1-150733006-G-T
• MyVariant Identifiers: chr1:g.150705482G>T (hg19) ; chr1:g.150733006G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733006G>T , CM000663.2:g.150733006G>T	GRCh38
NC_000001.10:g.150705482G>T , CM000663.1:g.150705482G>T	GRCh37
NC_000001.9:g.148972106G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*40C>A MANE Select	ENSP00000357981.3:n.*40C>A
ENST00000448301.7:c.*40C>A	ENSP00000408414.2:n.*40C>A
ENST00000472977.7:c.*40C>A	ENSP00000475176.2:n.*40C>A
ENST00000483930.2:c.*230C>A	ENSP00000475812.2:n.*230C>A
ENST00000607427.2:c.*40C>A	ENSP00000475557.2:n.*40C>A
ENST00000679512.1:c.*3C>A	ENSP00000505113.1:n.*3C>A
ENST00000679898.1:c.*40C>A	ENSP00000505326.1:n.*40C>A
ENST00000680288.1:c.*40C>A	ENSP00000506001.1:n.*40C>A
ENST00000680311.1:c.*119C>A	ENSP00000505020.1:n.*119C>A
ENST00000680471.1:c.*207C>A	ENSP00000506603.1:n.*207C>A
ENST00000680664.1:c.*40C>A	ENSP00000506248.1:n.*40C>A
ENST00000680931.1:c.*386C>A	ENSP00000504934.1:n.*386C>A
ENST00000681357.1:n.426C>A
ENST00000681444.1:c.*40C>A	ENSP00000505359.1:n.*40C>A
ENST00000368985.7:c.*40C>A	ENSP00000357981.3:n.*40C>A
ENST00000448301.6:c.*40C>A	ENSP00000408414.1:n.*40C>A
ENST00000472977.6:c.329C>A
ENST00000483930.1:c.584C>A	ENSP00000475812.1:n.584C>A
ENST00000607427.1:c.57C>A
NM_001199739.1:c.*40C>A	NP_001186668.1:n.*40C>A
NM_004079.4:c.*40C>A	NP_004070.3:n.*40C>A
NM_004079.5:c.*40C>A MANE Select	NP_004070.3:n.*40C>A
NM_001199739.2:c.*40C>A	NP_001186668.1:n.*40C>A