Canonical Allele Identifier: CA2573895606

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732977-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732977C>T , CM000663.2:g.150732977C>T	GRCh38
NC_000001.10:g.150705453C>T , CM000663.1:g.150705453C>T	GRCh37
NC_000001.9:g.148972077C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*69G>A MANE Select	ENSP00000357981.3:n.*69G>A
ENST00000448301.7:c.*69G>A	ENSP00000408414.2:n.*69G>A
ENST00000472977.7:c.*69G>A	ENSP00000475176.2:n.*69G>A
ENST00000483930.2:c.*259G>A	ENSP00000475812.2:n.*259G>A
ENST00000607427.2:c.*69G>A	ENSP00000475557.2:n.*69G>A
ENST00000679512.1:c.*32G>A	ENSP00000505113.1:n.*32G>A
ENST00000679898.1:c.*69G>A	ENSP00000505326.1:n.*69G>A
ENST00000680288.1:c.*69G>A	ENSP00000506001.1:n.*69G>A
ENST00000680311.1:c.*148G>A	ENSP00000505020.1:n.*148G>A
ENST00000680471.1:c.*236G>A	ENSP00000506603.1:n.*236G>A
ENST00000680664.1:c.*69G>A	ENSP00000506248.1:n.*69G>A
ENST00000680931.1:c.*415G>A	ENSP00000504934.1:n.*415G>A
ENST00000681357.1:n.455G>A
ENST00000681444.1:c.*69G>A	ENSP00000505359.1:n.*69G>A
ENST00000368985.7:c.*69G>A	ENSP00000357981.3:n.*69G>A
ENST00000448301.6:c.*69G>A	ENSP00000408414.1:n.*69G>A
ENST00000472977.6:c.358G>A
ENST00000483930.1:c.613G>A	ENSP00000475812.1:n.613G>A
ENST00000607427.1:c.86G>A
NM_001199739.1:c.*69G>A	NP_001186668.1:n.*69G>A
NM_004079.4:c.*69G>A	NP_004070.3:n.*69G>A
NM_004079.5:c.*69G>A MANE Select	NP_004070.3:n.*69G>A
NM_001199739.2:c.*69G>A	NP_001186668.1:n.*69G>A