Canonical Allele Identifier: CA2573895703
Gene: CTSS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150733025G>T , CM000663.2:g.150733025G>T GRCh38
NC_000001.10:g.150705501G>T , CM000663.1:g.150705501G>T GRCh37
NC_000001.9:g.148972125G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368985.8:c.*21C>A MANE Select ENSP00000357981.3:n.*21C>A
ENST00000448301.7:c.*21C>A ENSP00000408414.2:n.*21C>A
ENST00000472977.7:c.*21C>A ENSP00000475176.2:n.*21C>A
ENST00000483930.2:c.*211C>A ENSP00000475812.2:n.*211C>A
ENST00000607427.2:c.*21C>A ENSP00000475557.2:n.*21C>A
ENST00000679512.1:c.914C>A ENSP00000505113.1:p.Thr305Lys
ENST00000679898.1:c.*21C>A ENSP00000505326.1:n.*21C>A
ENST00000680288.1:c.*21C>A ENSP00000506001.1:n.*21C>A
ENST00000680311.1:c.*100C>A ENSP00000505020.1:n.*100C>A
ENST00000680471.1:c.*188C>A ENSP00000506603.1:n.*188C>A
ENST00000680664.1:c.*21C>A ENSP00000506248.1:n.*21C>A
ENST00000680931.1:c.*367C>A ENSP00000504934.1:n.*367C>A
ENST00000681357.1:n.407C>A
ENST00000681444.1:c.*21C>A ENSP00000505359.1:n.*21C>A
ENST00000368985.7:c.*21C>A ENSP00000357981.3:n.*21C>A
ENST00000448301.6:c.*21C>A ENSP00000408414.1:n.*21C>A
ENST00000472977.6:c.310C>A
ENST00000483930.1:c.565C>A ENSP00000475812.1:n.565C>A
ENST00000607427.1:c.38C>A
NM_001199739.1:c.*21C>A NP_001186668.1:n.*21C>A
NM_004079.4:c.*21C>A NP_004070.3:n.*21C>A
NM_004079.5:c.*21C>A MANE Select NP_004070.3:n.*21C>A
NM_001199739.2:c.*21C>A NP_001186668.1:n.*21C>A