Canonical Allele Identifier: CA2573895682

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733008-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733008T>C , CM000663.2:g.150733008T>C	GRCh38
NC_000001.10:g.150705484T>C , CM000663.1:g.150705484T>C	GRCh37
NC_000001.9:g.148972108T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*38A>G MANE Select	ENSP00000357981.3:n.*38A>G
ENST00000448301.7:c.*38A>G	ENSP00000408414.2:n.*38A>G
ENST00000472977.7:c.*38A>G	ENSP00000475176.2:n.*38A>G
ENST00000483930.2:c.*228A>G	ENSP00000475812.2:n.*228A>G
ENST00000607427.2:c.*38A>G	ENSP00000475557.2:n.*38A>G
ENST00000679512.1:c.*1A>G	ENSP00000505113.1:n.*1A>G
ENST00000679898.1:c.*38A>G	ENSP00000505326.1:n.*38A>G
ENST00000680288.1:c.*38A>G	ENSP00000506001.1:n.*38A>G
ENST00000680311.1:c.*117A>G	ENSP00000505020.1:n.*117A>G
ENST00000680471.1:c.*205A>G	ENSP00000506603.1:n.*205A>G
ENST00000680664.1:c.*38A>G	ENSP00000506248.1:n.*38A>G
ENST00000680931.1:c.*384A>G	ENSP00000504934.1:n.*384A>G
ENST00000681357.1:n.424A>G
ENST00000681444.1:c.*38A>G	ENSP00000505359.1:n.*38A>G
ENST00000368985.7:c.*38A>G	ENSP00000357981.3:n.*38A>G
ENST00000448301.6:c.*38A>G	ENSP00000408414.1:n.*38A>G
ENST00000472977.6:c.327A>G
ENST00000483930.1:c.582A>G	ENSP00000475812.1:n.582A>G
ENST00000607427.1:c.55A>G
NM_001199739.1:c.*38A>G	NP_001186668.1:n.*38A>G
NM_004079.4:c.*38A>G	NP_004070.3:n.*38A>G
NM_004079.5:c.*38A>G MANE Select	NP_004070.3:n.*38A>G
NM_001199739.2:c.*38A>G	NP_001186668.1:n.*38A>G