Canonical Allele Identifier: CA2647831711

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733037-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733037A>G , CM000663.2:g.150733037A>G	GRCh38
NC_000001.10:g.150705513A>G , CM000663.1:g.150705513A>G	GRCh37
NC_000001.9:g.148972137A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*9T>C MANE Select	ENSP00000357981.3:n.*9T>C
ENST00000448301.7:c.*9T>C	ENSP00000408414.2:n.*9T>C
ENST00000472977.7:c.*9T>C	ENSP00000475176.2:n.*9T>C
ENST00000483930.2:c.*199T>C	ENSP00000475812.2:n.*199T>C
ENST00000607427.2:c.*9T>C	ENSP00000475557.2:n.*9T>C
ENST00000679512.1:c.902T>C	ENSP00000505113.1:p.Leu301Pro
ENST00000679898.1:c.*9T>C	ENSP00000505326.1:n.*9T>C
ENST00000680288.1:c.*9T>C	ENSP00000506001.1:n.*9T>C
ENST00000680311.1:c.*88T>C	ENSP00000505020.1:n.*88T>C
ENST00000680471.1:c.*176T>C	ENSP00000506603.1:n.*176T>C
ENST00000680664.1:c.*9T>C	ENSP00000506248.1:n.*9T>C
ENST00000680931.1:c.*355T>C	ENSP00000504934.1:n.*355T>C
ENST00000681357.1:n.395T>C
ENST00000681444.1:c.*9T>C	ENSP00000505359.1:n.*9T>C
ENST00000368985.7:c.*9T>C	ENSP00000357981.3:n.*9T>C
ENST00000448301.6:c.*9T>C	ENSP00000408414.1:n.*9T>C
ENST00000472977.6:c.298T>C
ENST00000483930.1:c.553T>C	ENSP00000475812.1:n.553T>C
ENST00000607427.1:c.26T>C
NM_001199739.1:c.*9T>C	NP_001186668.1:n.*9T>C
NM_004079.4:c.*9T>C	NP_004070.3:n.*9T>C
NM_004079.5:c.*9T>C MANE Select	NP_004070.3:n.*9T>C
NM_001199739.2:c.*9T>C	NP_001186668.1:n.*9T>C