Canonical Allele Identifier: CA2647831700

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733023-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733023T>C , CM000663.2:g.150733023T>C	GRCh38
NC_000001.10:g.150705499T>C , CM000663.1:g.150705499T>C	GRCh37
NC_000001.9:g.148972123T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*23A>G MANE Select	ENSP00000357981.3:n.*23A>G
ENST00000448301.7:c.*23A>G	ENSP00000408414.2:n.*23A>G
ENST00000472977.7:c.*23A>G	ENSP00000475176.2:n.*23A>G
ENST00000483930.2:c.*213A>G	ENSP00000475812.2:n.*213A>G
ENST00000607427.2:c.*23A>G	ENSP00000475557.2:n.*23A>G
ENST00000679512.1:c.916A>G	ENSP00000505113.1:p.Asn306Asp
ENST00000679898.1:c.*23A>G	ENSP00000505326.1:n.*23A>G
ENST00000680288.1:c.*23A>G	ENSP00000506001.1:n.*23A>G
ENST00000680311.1:c.*102A>G	ENSP00000505020.1:n.*102A>G
ENST00000680471.1:c.*190A>G	ENSP00000506603.1:n.*190A>G
ENST00000680664.1:c.*23A>G	ENSP00000506248.1:n.*23A>G
ENST00000680931.1:c.*369A>G	ENSP00000504934.1:n.*369A>G
ENST00000681357.1:n.409A>G
ENST00000681444.1:c.*23A>G	ENSP00000505359.1:n.*23A>G
ENST00000368985.7:c.*23A>G	ENSP00000357981.3:n.*23A>G
ENST00000448301.6:c.*23A>G	ENSP00000408414.1:n.*23A>G
ENST00000472977.6:c.312A>G
ENST00000483930.1:c.567A>G	ENSP00000475812.1:n.567A>G
ENST00000607427.1:c.40A>G
NM_001199739.1:c.*23A>G	NP_001186668.1:n.*23A>G
NM_004079.4:c.*23A>G	NP_004070.3:n.*23A>G
NM_004079.5:c.*23A>G MANE Select	NP_004070.3:n.*23A>G
NM_001199739.2:c.*23A>G	NP_001186668.1:n.*23A>G