Canonical Allele Identifier: CA2647831712

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733039-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733039A>G , CM000663.2:g.150733039A>G	GRCh38
NC_000001.10:g.150705515A>G , CM000663.1:g.150705515A>G	GRCh37
NC_000001.9:g.148972139A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*7T>C MANE Select	ENSP00000357981.3:n.*7T>C
ENST00000448301.7:c.*7T>C	ENSP00000408414.2:n.*7T>C
ENST00000472977.7:c.*7T>C	ENSP00000475176.2:n.*7T>C
ENST00000483930.2:c.*197T>C	ENSP00000475812.2:n.*197T>C
ENST00000607427.2:c.*7T>C	ENSP00000475557.2:n.*7T>C
ENST00000679512.1:c.900T>C	ENSP00000505113.1:p.Ser300=
ENST00000679898.1:c.*7T>C	ENSP00000505326.1:n.*7T>C
ENST00000680288.1:c.*7T>C	ENSP00000506001.1:n.*7T>C
ENST00000680311.1:c.*86T>C	ENSP00000505020.1:n.*86T>C
ENST00000680471.1:c.*174T>C	ENSP00000506603.1:n.*174T>C
ENST00000680664.1:c.*7T>C	ENSP00000506248.1:n.*7T>C
ENST00000680931.1:c.*353T>C	ENSP00000504934.1:n.*353T>C
ENST00000681357.1:n.393T>C
ENST00000681444.1:c.*7T>C	ENSP00000505359.1:n.*7T>C
ENST00000368985.7:c.*7T>C	ENSP00000357981.3:n.*7T>C
ENST00000448301.6:c.*7T>C	ENSP00000408414.1:n.*7T>C
ENST00000472977.6:c.296T>C
ENST00000483930.1:c.551T>C	ENSP00000475812.1:n.551T>C
ENST00000607427.1:c.24T>C
NM_001199739.1:c.*7T>C	NP_001186668.1:n.*7T>C
NM_004079.4:c.*7T>C	NP_004070.3:n.*7T>C
NM_004079.5:c.*7T>C MANE Select	NP_004070.3:n.*7T>C
NM_001199739.2:c.*7T>C	NP_001186668.1:n.*7T>C