Canonical Allele Identifier: CA2647831698

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733020-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733020G>T , CM000663.2:g.150733020G>T	GRCh38
NC_000001.10:g.150705496G>T , CM000663.1:g.150705496G>T	GRCh37
NC_000001.9:g.148972120G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.*26C>A MANE Select	ENSP00000357981.3:n.*26C>A
ENST00000448301.7:c.*26C>A	ENSP00000408414.2:n.*26C>A
ENST00000472977.7:c.*26C>A	ENSP00000475176.2:n.*26C>A
ENST00000483930.2:c.*216C>A	ENSP00000475812.2:n.*216C>A
ENST00000607427.2:c.*26C>A	ENSP00000475557.2:n.*26C>A
ENST00000679512.1:c.919C>A	ENSP00000505113.1:p.Gln307Lys
ENST00000679898.1:c.*26C>A	ENSP00000505326.1:n.*26C>A
ENST00000680288.1:c.*26C>A	ENSP00000506001.1:n.*26C>A
ENST00000680311.1:c.*105C>A	ENSP00000505020.1:n.*105C>A
ENST00000680471.1:c.*193C>A	ENSP00000506603.1:n.*193C>A
ENST00000680664.1:c.*26C>A	ENSP00000506248.1:n.*26C>A
ENST00000680931.1:c.*372C>A	ENSP00000504934.1:n.*372C>A
ENST00000681357.1:n.412C>A
ENST00000681444.1:c.*26C>A	ENSP00000505359.1:n.*26C>A
ENST00000368985.7:c.*26C>A	ENSP00000357981.3:n.*26C>A
ENST00000448301.6:c.*26C>A	ENSP00000408414.1:n.*26C>A
ENST00000472977.6:c.315C>A
ENST00000483930.1:c.570C>A	ENSP00000475812.1:n.570C>A
ENST00000607427.1:c.43C>A
NM_001199739.1:c.*26C>A	NP_001186668.1:n.*26C>A
NM_004079.4:c.*26C>A	NP_004070.3:n.*26C>A
NM_004079.5:c.*26C>A MANE Select	NP_004070.3:n.*26C>A
NM_001199739.2:c.*26C>A	NP_001186668.1:n.*26C>A