Canonical Allele Identifier: CA1007645324

Gene: CTSS

Linked Data

• dbSNP Id: rs1652556240
• gnomAD v3: 1-150732983-GA-G
• gnomAD v4: 1-150732983-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732988del , CM000663.2:g.150732988del	GRCh38
NC_000001.10:g.150705464del , CM000663.1:g.150705464del	GRCh37
NC_000001.9:g.148972088del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*62del MANE Select	ENSP00000357981.3:n.*62del
ENST00000448301.7:c.*62del	ENSP00000408414.2:n.*62del
ENST00000472977.7:c.*62del	ENSP00000475176.2:n.*62del
ENST00000483930.2:c.*252del	ENSP00000475812.2:n.*252del
ENST00000607427.2:c.*62del	ENSP00000475557.2:n.*62del
ENST00000679512.1:c.*25del	ENSP00000505113.1:n.*25del
ENST00000679898.1:c.*62del	ENSP00000505326.1:n.*62del
ENST00000680288.1:c.*62del	ENSP00000506001.1:n.*62del
ENST00000680311.1:c.*141del	ENSP00000505020.1:n.*141del
ENST00000680471.1:c.*229del	ENSP00000506603.1:n.*229del
ENST00000680664.1:c.*62del	ENSP00000506248.1:n.*62del
ENST00000680931.1:c.*408del	ENSP00000504934.1:n.*408del
ENST00000681357.1:n.448del
ENST00000681444.1:c.*62del	ENSP00000505359.1:n.*62del
ENST00000368985.7:c.*62del	ENSP00000357981.3:n.*62del
ENST00000448301.6:c.*62del	ENSP00000408414.1:n.*62del
ENST00000472977.6:c.351del
ENST00000483930.1:c.606del	ENSP00000475812.1:n.606del
ENST00000607427.1:c.79del
NM_001199739.1:c.*62del	NP_001186668.1:n.*62del
NM_004079.4:c.*62del	NP_004070.3:n.*62del
NM_004079.5:c.*62del MANE Select	NP_004070.3:n.*62del
NM_001199739.2:c.*62del	NP_001186668.1:n.*62del