Canonical Allele Identifier: CA2647831692

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732999-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732999A>G , CM000663.2:g.150732999A>G	GRCh38
NC_000001.10:g.150705475A>G , CM000663.1:g.150705475A>G	GRCh37
NC_000001.9:g.148972099A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*47T>C MANE Select	ENSP00000357981.3:n.*47T>C
ENST00000448301.7:c.*47T>C	ENSP00000408414.2:n.*47T>C
ENST00000472977.7:c.*47T>C	ENSP00000475176.2:n.*47T>C
ENST00000483930.2:c.*237T>C	ENSP00000475812.2:n.*237T>C
ENST00000607427.2:c.*47T>C	ENSP00000475557.2:n.*47T>C
ENST00000679512.1:c.*10T>C	ENSP00000505113.1:n.*10T>C
ENST00000679898.1:c.*47T>C	ENSP00000505326.1:n.*47T>C
ENST00000680288.1:c.*47T>C	ENSP00000506001.1:n.*47T>C
ENST00000680311.1:c.*126T>C	ENSP00000505020.1:n.*126T>C
ENST00000680471.1:c.*214T>C	ENSP00000506603.1:n.*214T>C
ENST00000680664.1:c.*47T>C	ENSP00000506248.1:n.*47T>C
ENST00000680931.1:c.*393T>C	ENSP00000504934.1:n.*393T>C
ENST00000681357.1:n.433T>C
ENST00000681444.1:c.*47T>C	ENSP00000505359.1:n.*47T>C
ENST00000368985.7:c.*47T>C	ENSP00000357981.3:n.*47T>C
ENST00000448301.6:c.*47T>C	ENSP00000408414.1:n.*47T>C
ENST00000472977.6:c.336T>C
ENST00000483930.1:c.591T>C	ENSP00000475812.1:n.591T>C
ENST00000607427.1:c.64T>C
NM_001199739.1:c.*47T>C	NP_001186668.1:n.*47T>C
NM_004079.4:c.*47T>C	NP_004070.3:n.*47T>C
NM_004079.5:c.*47T>C MANE Select	NP_004070.3:n.*47T>C
NM_001199739.2:c.*47T>C	NP_001186668.1:n.*47T>C