Canonical Allele Identifier: CA2647831678

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732967-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732967C>A , CM000663.2:g.150732967C>A	GRCh38
NC_000001.10:g.150705443C>A , CM000663.1:g.150705443C>A	GRCh37
NC_000001.9:g.148972067C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*79G>T MANE Select	ENSP00000357981.3:n.*79G>T
ENST00000448301.7:c.*79G>T	ENSP00000408414.2:n.*79G>T
ENST00000472977.7:c.*79G>T	ENSP00000475176.2:n.*79G>T
ENST00000483930.2:c.*269G>T	ENSP00000475812.2:n.*269G>T
ENST00000607427.2:c.*79G>T	ENSP00000475557.2:n.*79G>T
ENST00000679512.1:c.*42G>T	ENSP00000505113.1:n.*42G>T
ENST00000679898.1:c.*79G>T	ENSP00000505326.1:n.*79G>T
ENST00000680288.1:c.*79G>T	ENSP00000506001.1:n.*79G>T
ENST00000680311.1:c.*158G>T	ENSP00000505020.1:n.*158G>T
ENST00000680471.1:c.*246G>T	ENSP00000506603.1:n.*246G>T
ENST00000680664.1:c.*79G>T	ENSP00000506248.1:n.*79G>T
ENST00000680931.1:c.*425G>T	ENSP00000504934.1:n.*425G>T
ENST00000681357.1:n.465G>T
ENST00000681444.1:c.*79G>T	ENSP00000505359.1:n.*79G>T
ENST00000368985.7:c.*79G>T	ENSP00000357981.3:n.*79G>T
ENST00000448301.6:c.*79G>T	ENSP00000408414.1:n.*79G>T
ENST00000472977.6:c.368G>T
ENST00000483930.1:c.623G>T	ENSP00000475812.1:n.623G>T
ENST00000607427.1:c.96G>T
NM_001199739.1:c.*79G>T	NP_001186668.1:n.*79G>T
NM_004079.4:c.*79G>T	NP_004070.3:n.*79G>T
NM_004079.5:c.*79G>T MANE Select	NP_004070.3:n.*79G>T
NM_001199739.2:c.*79G>T	NP_001186668.1:n.*79G>T