Canonical Allele Identifier: CA2647831685

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732992-AGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732993_150732995del , CM000663.2:g.150732993_150732995del	GRCh38
NC_000001.10:g.150705469_150705471del , CM000663.1:g.150705469_150705471del	GRCh37
NC_000001.9:g.148972093_148972095del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*51_*53del MANE Select	ENSP00000357981.3:n.*51_*53del
ENST00000448301.7:c.*51_*53del	ENSP00000408414.2:n.*51_*53del
ENST00000472977.7:c.*51_*53del	ENSP00000475176.2:n.*51_*53del
ENST00000483930.2:c.*241_*243del	ENSP00000475812.2:n.*241_*243del
ENST00000607427.2:c.*51_*53del	ENSP00000475557.2:n.*51_*53del
ENST00000679512.1:c.*14_*16del	ENSP00000505113.1:n.*14_*16del
ENST00000679898.1:c.*51_*53del	ENSP00000505326.1:n.*51_*53del
ENST00000680288.1:c.*51_*53del	ENSP00000506001.1:n.*51_*53del
ENST00000680311.1:c.*130_*132del	ENSP00000505020.1:n.*130_*132del
ENST00000680471.1:c.*218_*220del	ENSP00000506603.1:n.*218_*220del
ENST00000680664.1:c.*51_*53del	ENSP00000506248.1:n.*51_*53del
ENST00000680931.1:c.*397_*399del	ENSP00000504934.1:n.*397_*399del
ENST00000681357.1:n.437_439del
ENST00000681444.1:c.*51_*53del	ENSP00000505359.1:n.*51_*53del
ENST00000368985.7:c.*51_*53del	ENSP00000357981.3:n.*51_*53del
ENST00000448301.6:c.*51_*53del	ENSP00000408414.1:n.*51_*53del
ENST00000472977.6:c.340_342del
ENST00000483930.1:c.595_597del	ENSP00000475812.1:n.595_597del
ENST00000607427.1:c.68_70del
NM_001199739.1:c.*51_*53del	NP_001186668.1:n.*51_*53del
NM_004079.4:c.*51_*53del	NP_004070.3:n.*51_*53del
NM_004079.5:c.*51_*53del MANE Select	NP_004070.3:n.*51_*53del
NM_001199739.2:c.*51_*53del	NP_001186668.1:n.*51_*53del