Canonical Allele Identifier: CA2479286166

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732977_150732978delinsCA , CM000663.2:g.150732977_150732978delinsCA	GRCh38
NC_000001.10:g.150705453_150705454delinsCA , CM000663.1:g.150705453_150705454delinsCA	GRCh37
NC_000001.9:g.148972077_148972078delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*68_*69delinsTG MANE Select	ENSP00000357981.3:n.*68_*69delinsTG
ENST00000448301.7:c.*68_*69delinsTG	ENSP00000408414.2:n.*68_*69delinsTG
ENST00000472977.7:c.*68_*69delinsTG	ENSP00000475176.2:n.*68_*69delinsTG
ENST00000483930.2:c.*258_*259delinsTG	ENSP00000475812.2:n.*258_*259delinsTG
ENST00000607427.2:c.*68_*69delinsTG	ENSP00000475557.2:n.*68_*69delinsTG
ENST00000679512.1:c.*31_*32delinsTG	ENSP00000505113.1:n.*31_*32delinsTG
ENST00000679898.1:c.*68_*69delinsTG	ENSP00000505326.1:n.*68_*69delinsTG
ENST00000680288.1:c.*68_*69delinsTG	ENSP00000506001.1:n.*68_*69delinsTG
ENST00000680311.1:c.*147_*148delinsTG	ENSP00000505020.1:n.*147_*148delinsTG
ENST00000680471.1:c.*235_*236delinsTG	ENSP00000506603.1:n.*235_*236delinsTG
ENST00000680664.1:c.*68_*69delinsTG	ENSP00000506248.1:n.*68_*69delinsTG
ENST00000680931.1:c.*414_*415delinsTG	ENSP00000504934.1:n.*414_*415delinsTG
ENST00000681357.1:n.454_455delinsTG
ENST00000681444.1:c.*68_*69delinsTG	ENSP00000505359.1:n.*68_*69delinsTG
ENST00000368985.7:c.*68_*69delinsTG	ENSP00000357981.3:n.*68_*69delinsTG
ENST00000448301.6:c.*68_*69delinsTG	ENSP00000408414.1:n.*68_*69delinsTG
ENST00000472977.6:c.357_358delinsTG
ENST00000483930.1:c.612_613delinsTG	ENSP00000475812.1:n.612_613delinsTG
ENST00000607427.1:c.85_86delinsTG
NM_001199739.1:c.*68_*69delinsTG	NP_001186668.1:n.*68_*69delinsTG
NM_004079.4:c.*68_*69delinsTG	NP_004070.3:n.*68_*69delinsTG
NM_004079.5:c.*68_*69delinsTG MANE Select	NP_004070.3:n.*68_*69delinsTG
NM_001199739.2:c.*68_*69delinsTG	NP_001186668.1:n.*68_*69delinsTG