Canonical Allele Identifier: CA2697408534

Gene: CTSS

Linked Data

• dbSNP Id: rs2101907234

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733036G>A , CM000663.2:g.150733036G>A	GRCh38
NC_000001.10:g.150705512G>A , CM000663.1:g.150705512G>A	GRCh37
NC_000001.9:g.148972136G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*10C>T MANE Select	ENSP00000357981.3:n.*10C>T
ENST00000448301.7:c.*10C>T	ENSP00000408414.2:n.*10C>T
ENST00000472977.7:c.*10C>T	ENSP00000475176.2:n.*10C>T
ENST00000483930.2:c.*200C>T	ENSP00000475812.2:n.*200C>T
ENST00000607427.2:c.*10C>T	ENSP00000475557.2:n.*10C>T
ENST00000679512.1:c.903C>T	ENSP00000505113.1:p.Leu301=
ENST00000679898.1:c.*10C>T	ENSP00000505326.1:n.*10C>T
ENST00000680288.1:c.*10C>T	ENSP00000506001.1:n.*10C>T
ENST00000680311.1:c.*89C>T	ENSP00000505020.1:n.*89C>T
ENST00000680471.1:c.*177C>T	ENSP00000506603.1:n.*177C>T
ENST00000680664.1:c.*10C>T	ENSP00000506248.1:n.*10C>T
ENST00000680931.1:c.*356C>T	ENSP00000504934.1:n.*356C>T
ENST00000681357.1:n.396C>T
ENST00000681444.1:c.*10C>T	ENSP00000505359.1:n.*10C>T
ENST00000368985.7:c.*10C>T	ENSP00000357981.3:n.*10C>T
ENST00000448301.6:c.*10C>T	ENSP00000408414.1:n.*10C>T
ENST00000472977.6:c.299C>T
ENST00000483930.1:c.554C>T	ENSP00000475812.1:n.554C>T
ENST00000607427.1:c.27C>T
NM_001199739.1:c.*10C>T	NP_001186668.1:n.*10C>T
NM_004079.4:c.*10C>T	NP_004070.3:n.*10C>T
NM_004079.5:c.*10C>T MANE Select	NP_004070.3:n.*10C>T
NM_001199739.2:c.*10C>T	NP_001186668.1:n.*10C>T