Canonical Allele Identifier: CA342322419
Gene: CTSS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150733104G>C , CM000663.2:g.150733104G>C GRCh38
NC_000001.10:g.150705580G>C , CM000663.1:g.150705580G>C GRCh37
NC_000001.9:g.148972204G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368985.8:c.938C>G MANE Select ENSP00000357981.3:p.Ala313Gly
ENST00000448301.7:c.710C>G ENSP00000408414.2:p.Ala237Gly
ENST00000472977.7:c.938C>G ENSP00000475176.2:p.Ala313Gly
ENST00000483930.2:c.*132C>G ENSP00000475812.2:n.*132C>G
ENST00000607427.2:c.938C>G ENSP00000475557.2:p.Ala313Gly
ENST00000679512.1:c.835C>G ENSP00000505113.1:p.Gln279Glu
ENST00000679898.1:c.665C>G ENSP00000505326.1:p.Ala222Gly
ENST00000680288.1:c.788C>G ENSP00000506001.1:p.Ala263Gly
ENST00000680311.1:c.*21C>G ENSP00000505020.1:n.*21C>G
ENST00000680471.1:c.*109C>G ENSP00000506603.1:n.*109C>G
ENST00000680664.1:c.761C>G ENSP00000506248.1:p.Ala254Gly
ENST00000680931.1:c.*288C>G ENSP00000504934.1:n.*288C>G
ENST00000681357.1:n.328C>G
ENST00000681444.1:c.938C>G ENSP00000505359.1:p.Ala313Gly
ENST00000368985.7:c.938C>G ENSP00000357981.3:p.Ala313Gly
ENST00000448301.6:c.788C>G ENSP00000408414.1:p.Ala263Gly
ENST00000472977.6:c.231C>G
ENST00000483930.1:c.486C>G ENSP00000475812.1:n.486C>G
NM_001199739.1:c.788C>G NP_001186668.1:p.Ala263Gly
NM_004079.4:c.938C>G NP_004070.3:p.Ala313Gly
NM_004079.5:c.938C>G MANE Select NP_004070.3:p.Ala313Gly
NM_001199739.2:c.788C>G NP_001186668.1:p.Ala263Gly