Canonical Allele Identifier: CA526062651

Gene: CTSS

Linked Data

• dbSNP Id: rs1286094287
• gnomAD v2: 1-150705464-ATTAAG-A
• gnomAD v3: 1-150732988-ATTAAG-A
• gnomAD v4: 1-150732988-ATTAAG-A
• MyVariant Identifiers: chr1:g.150705465_150705469del (hg19) ; chr1:g.150732989_150732993del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732994_150732998del , CM000663.2:g.150732994_150732998del	GRCh38
NC_000001.10:g.150705470_150705474del , CM000663.1:g.150705470_150705474del	GRCh37
NC_000001.9:g.148972094_148972098del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*53_*57del MANE Select	ENSP00000357981.3:n.*53_*57del
ENST00000448301.7:c.*53_*57del	ENSP00000408414.2:n.*53_*57del
ENST00000472977.7:c.*53_*57del	ENSP00000475176.2:n.*53_*57del
ENST00000483930.2:c.*243_*247del	ENSP00000475812.2:n.*243_*247del
ENST00000607427.2:c.*53_*57del	ENSP00000475557.2:n.*53_*57del
ENST00000679512.1:c.*16_*20del	ENSP00000505113.1:n.*16_*20del
ENST00000679898.1:c.*53_*57del	ENSP00000505326.1:n.*53_*57del
ENST00000680288.1:c.*53_*57del	ENSP00000506001.1:n.*53_*57del
ENST00000680311.1:c.*132_*136del	ENSP00000505020.1:n.*132_*136del
ENST00000680471.1:c.*220_*224del	ENSP00000506603.1:n.*220_*224del
ENST00000680664.1:c.*53_*57del	ENSP00000506248.1:n.*53_*57del
ENST00000680931.1:c.*399_*403del	ENSP00000504934.1:n.*399_*403del
ENST00000681357.1:n.439_443del
ENST00000681444.1:c.*53_*57del	ENSP00000505359.1:n.*53_*57del
ENST00000368985.7:c.*53_*57del	ENSP00000357981.3:n.*53_*57del
ENST00000448301.6:c.*53_*57del	ENSP00000408414.1:n.*53_*57del
ENST00000472977.6:c.342_346del
ENST00000483930.1:c.597_601del	ENSP00000475812.1:n.597_601del
ENST00000607427.1:c.70_74del
NM_001199739.1:c.*53_*57del	NP_001186668.1:n.*53_*57del
NM_004079.4:c.*53_*57del	NP_004070.3:n.*53_*57del
NM_004079.5:c.*53_*57del MANE Select	NP_004070.3:n.*53_*57del
NM_001199739.2:c.*53_*57del	NP_001186668.1:n.*53_*57del