Canonical Allele Identifier: CA2479286277

Gene: CTSS

Linked Data

• dbSNP Id: rs1652566072

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733380_150733381insTAA , CM000663.2:g.150733380_150733381insTAA	GRCh38
NC_000001.10:g.150705856_150705857insTAA , CM000663.1:g.150705856_150705857insTAA	GRCh37
NC_000001.9:g.148972480_148972481insTAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.897-235_897-234insTAT MANE Select	ENSP00000357981.3:n.897-235_897-234insTAT
ENST00000448301.7:c.669-235_669-234insTAT	ENSP00000408414.2:n.669-235_669-234insTAT
ENST00000472977.7:c.897-235_897-234insTAT	ENSP00000475176.2:n.897-235_897-234insTAT
ENST00000483930.2:c.*91-235_*91-234insTAT	ENSP00000475812.2:n.*91-235_*91-234insTAT
ENST00000607427.2:c.897-235_897-234insTAT	ENSP00000475557.2:n.897-235_897-234insTAT
ENST00000679512.1:c.794-235_794-234insTAT	ENSP00000505113.1:n.794-235_794-234insTAT
ENST00000679898.1:c.624-235_624-234insTAT	ENSP00000505326.1:n.624-235_624-234insTAT
ENST00000680288.1:c.747-235_747-234insTAT	ENSP00000506001.1:n.747-235_747-234insTAT
ENST00000680311.1:c.628-235_628-234insTAT	ENSP00000505020.1:n.628-235_628-234insTAT
ENST00000680471.1:c.*68-235_*68-234insTAT	ENSP00000506603.1:n.*68-235_*68-234insTAT
ENST00000680664.1:c.720-235_720-234insTAT	ENSP00000506248.1:n.720-235_720-234insTAT
ENST00000680931.1:c.*247-235_*247-234insTAT	ENSP00000504934.1:n.*247-235_*247-234insTAT
ENST00000681357.1:n.287-235_287-234insTAT
ENST00000681444.1:c.897-235_897-234insTAT	ENSP00000505359.1:n.897-235_897-234insTAT
ENST00000368985.7:c.897-235_897-234insTAT	ENSP00000357981.3:n.897-235_897-234insTAT
ENST00000448301.6:c.747-235_747-234insTAT	ENSP00000408414.1:n.747-235_747-234insTAT
ENST00000472977.6:c.190-235_190-234insTAT
ENST00000483930.1:c.445-235_445-234insTAT	ENSP00000475812.1:n.445-235_445-234insTAT
NM_001199739.1:c.747-235_747-234insTAT	NP_001186668.1:n.747-235_747-234insTAT
NM_004079.4:c.897-235_897-234insTAT	NP_004070.3:n.897-235_897-234insTAT
NM_004079.5:c.897-235_897-234insTAT MANE Select	NP_004070.3:n.897-235_897-234insTAT
NM_001199739.2:c.747-235_747-234insTAT	NP_001186668.1:n.747-235_747-234insTAT