Canonical Allele Identifier: CA645930878

Gene: CTSS

Linked Data

• COSMIC: COSN7177087

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733040G>C , CM000663.2:g.150733040G>C	GRCh38
NC_000001.10:g.150705516G>C , CM000663.1:g.150705516G>C	GRCh37
NC_000001.9:g.148972140G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.*6C>G MANE Select	ENSP00000357981.3:n.*6C>G
ENST00000448301.7:c.*6C>G	ENSP00000408414.2:n.*6C>G
ENST00000472977.7:c.*6C>G	ENSP00000475176.2:n.*6C>G
ENST00000483930.2:c.*196C>G	ENSP00000475812.2:n.*196C>G
ENST00000607427.2:c.*6C>G	ENSP00000475557.2:n.*6C>G
ENST00000679512.1:c.899C>G	ENSP00000505113.1:p.Ser300Cys
ENST00000679898.1:c.*6C>G	ENSP00000505326.1:n.*6C>G
ENST00000680288.1:c.*6C>G	ENSP00000506001.1:n.*6C>G
ENST00000680311.1:c.*85C>G	ENSP00000505020.1:n.*85C>G
ENST00000680471.1:c.*173C>G	ENSP00000506603.1:n.*173C>G
ENST00000680664.1:c.*6C>G	ENSP00000506248.1:n.*6C>G
ENST00000680931.1:c.*352C>G	ENSP00000504934.1:n.*352C>G
ENST00000681357.1:n.392C>G
ENST00000681444.1:c.*6C>G	ENSP00000505359.1:n.*6C>G
ENST00000368985.7:c.*6C>G	ENSP00000357981.3:n.*6C>G
ENST00000448301.6:c.*6C>G	ENSP00000408414.1:n.*6C>G
ENST00000472977.6:c.295C>G
ENST00000483930.1:c.550C>G	ENSP00000475812.1:n.550C>G
ENST00000607427.1:c.23C>G
NM_001199739.1:c.*6C>G	NP_001186668.1:n.*6C>G
NM_004079.4:c.*6C>G	NP_004070.3:n.*6C>G
NM_004079.5:c.*6C>G MANE Select	NP_004070.3:n.*6C>G
NM_001199739.2:c.*6C>G	NP_001186668.1:n.*6C>G