Canonical Allele Identifier: CA10780914
Gene: CTSS HGNC NCBI

Linked Data

dbSNP Id: rs1136774

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150765721C>T , CM000663.2:g.150765721C>T GRCh38
NC_000001.10:g.150738197C>T , CM000663.1:g.150738197C>T GRCh37
NC_000001.9:g.149004821C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368985.8:c.-25G>A MANE Select ENSP00000357981.3:n.-25G>A
ENST00000448301.7:c.-25G>A ENSP00000408414.2:n.-25G>A
ENST00000472977.7:c.-25G>A ENSP00000475176.2:n.-25G>A
ENST00000480760.2:n.83G>A
ENST00000483930.2:c.-25G>A ENSP00000475812.2:n.-25G>A
ENST00000607427.2:c.-25G>A ENSP00000475557.2:n.-25G>A
ENST00000679512.1:c.-25G>A ENSP00000505113.1:n.-25G>A
ENST00000679582.1:c.-25G>A ENSP00000504885.1:n.-25G>A
ENST00000679898.1:c.-25G>A ENSP00000505326.1:n.-25G>A
ENST00000680288.1:c.-25G>A ENSP00000506001.1:n.-25G>A
ENST00000680311.1:c.-25G>A ENSP00000505020.1:n.-25G>A
ENST00000680466.1:n.45G>A
ENST00000680471.1:c.-25G>A ENSP00000506603.1:n.-25G>A
ENST00000680664.1:c.-75G>A ENSP00000506248.1:n.-75G>A
ENST00000680931.1:c.-25G>A ENSP00000504934.1:n.-25G>A
ENST00000681444.1:c.-25G>A ENSP00000505359.1:n.-25G>A
ENST00000681728.1:c.-25G>A ENSP00000505313.1:n.-25G>A
ENST00000681863.1:n.124G>A
ENST00000368985.7:c.-25G>A ENSP00000357981.3:n.-25G>A
ENST00000448301.6:c.-25G>A ENSP00000408414.1:n.-25G>A
NM_001199739.1:c.-25G>A NP_001186668.1:n.-25G>A
NM_004079.4:c.-25G>A NP_004070.3:n.-25G>A
NM_004079.5:c.-25G>A MANE Select NP_004070.3:n.-25G>A
NM_001199739.2:c.-25G>A NP_001186668.1:n.-25G>A