Canonical Allele Identifier: CA420696539

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705522C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733046C>T , CM000663.2:g.150733046C>T	GRCh38
NC_000001.10:g.150705522C>T , CM000663.1:g.150705522C>T	GRCh37
NC_000001.9:g.148972146C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.996G>A MANE Select	ENSP00000357981.3:p.Ter332=
ENST00000448301.7:c.768G>A	ENSP00000408414.2:p.Ter256=
ENST00000472977.7:c.996G>A	ENSP00000475176.2:p.Ter332=
ENST00000483930.2:c.*190G>A	ENSP00000475812.2:n.*190G>A
ENST00000607427.2:c.996G>A	ENSP00000475557.2:p.Ter332=
ENST00000679512.1:c.893G>A	ENSP00000505113.1:p.Arg298Lys
ENST00000679898.1:c.723G>A	ENSP00000505326.1:p.Ter241=
ENST00000680288.1:c.846G>A	ENSP00000506001.1:p.Ter282=
ENST00000680311.1:c.*79G>A	ENSP00000505020.1:n.*79G>A
ENST00000680471.1:c.*167G>A	ENSP00000506603.1:n.*167G>A
ENST00000680664.1:c.819G>A	ENSP00000506248.1:p.Ter273=
ENST00000680931.1:c.*346G>A	ENSP00000504934.1:n.*346G>A
ENST00000681357.1:n.386G>A
ENST00000681444.1:c.996G>A	ENSP00000505359.1:p.Ter332=
ENST00000368985.7:c.996G>A	ENSP00000357981.3:p.Ter332=
ENST00000448301.6:c.846G>A	ENSP00000408414.1:p.Ter282=
ENST00000472977.6:c.289G>A
ENST00000483930.1:c.544G>A	ENSP00000475812.1:n.544G>A
ENST00000607427.1:c.17G>A
NM_001199739.1:c.846G>A	NP_001186668.1:p.Ter282=
NM_004079.4:c.996G>A	NP_004070.3:p.Ter332=
NM_004079.5:c.996G>A MANE Select	NP_004070.3:p.Ter332=
NM_001199739.2:c.846G>A	NP_001186668.1:p.Ter282=