Canonical Allele Identifier: CA2647831679

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732968-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732970_150732971del , CM000663.2:g.150732970_150732971del	GRCh38
NC_000001.10:g.150705446_150705447del , CM000663.1:g.150705446_150705447del	GRCh37
NC_000001.9:g.148972070_148972071del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*76_*77del MANE Select	ENSP00000357981.3:n.*76_*77del
ENST00000448301.7:c.*76_*77del	ENSP00000408414.2:n.*76_*77del
ENST00000472977.7:c.*76_*77del	ENSP00000475176.2:n.*76_*77del
ENST00000483930.2:c.*266_*267del	ENSP00000475812.2:n.*266_*267del
ENST00000607427.2:c.*76_*77del	ENSP00000475557.2:n.*76_*77del
ENST00000679512.1:c.*39_*40del	ENSP00000505113.1:n.*39_*40del
ENST00000679898.1:c.*76_*77del	ENSP00000505326.1:n.*76_*77del
ENST00000680288.1:c.*76_*77del	ENSP00000506001.1:n.*76_*77del
ENST00000680311.1:c.*155_*156del	ENSP00000505020.1:n.*155_*156del
ENST00000680471.1:c.*243_*244del	ENSP00000506603.1:n.*243_*244del
ENST00000680664.1:c.*76_*77del	ENSP00000506248.1:n.*76_*77del
ENST00000680931.1:c.*422_*423del	ENSP00000504934.1:n.*422_*423del
ENST00000681357.1:n.462_463del
ENST00000681444.1:c.*76_*77del	ENSP00000505359.1:n.*76_*77del
ENST00000368985.7:c.*76_*77del	ENSP00000357981.3:n.*76_*77del
ENST00000448301.6:c.*76_*77del	ENSP00000408414.1:n.*76_*77del
ENST00000472977.6:c.365_366del
ENST00000483930.1:c.620_621del	ENSP00000475812.1:n.620_621del
ENST00000607427.1:c.93_94del
NM_001199739.1:c.*76_*77del	NP_001186668.1:n.*76_*77del
NM_004079.4:c.*76_*77del	NP_004070.3:n.*76_*77del
NM_004079.5:c.*76_*77del MANE Select	NP_004070.3:n.*76_*77del
NM_001199739.2:c.*76_*77del	NP_001186668.1:n.*76_*77del