Canonical Allele Identifier: CA420696576

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733111-G-T
• MyVariant Identifiers: chr1:g.150705587G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733111G>T , CM000663.2:g.150733111G>T	GRCh38
NC_000001.10:g.150705587G>T , CM000663.1:g.150705587G>T	GRCh37
NC_000001.9:g.148972211G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.931C>A MANE Select	ENSP00000357981.3:p.Arg311=
ENST00000448301.7:c.703C>A	ENSP00000408414.2:p.Arg235=
ENST00000472977.7:c.931C>A	ENSP00000475176.2:p.Arg311=
ENST00000483930.2:c.*125C>A	ENSP00000475812.2:n.*125C>A
ENST00000607427.2:c.931C>A	ENSP00000475557.2:p.Arg311=
ENST00000679512.1:c.828C>A	ENSP00000505113.1:p.Phe276Leu
ENST00000679898.1:c.658C>A	ENSP00000505326.1:p.Arg220=
ENST00000680288.1:c.781C>A	ENSP00000506001.1:p.Arg261=
ENST00000680311.1:c.*14C>A	ENSP00000505020.1:n.*14C>A
ENST00000680471.1:c.*102C>A	ENSP00000506603.1:n.*102C>A
ENST00000680664.1:c.754C>A	ENSP00000506248.1:p.Arg252=
ENST00000680931.1:c.*281C>A	ENSP00000504934.1:n.*281C>A
ENST00000681357.1:n.321C>A
ENST00000681444.1:c.931C>A	ENSP00000505359.1:p.Arg311=
ENST00000368985.7:c.931C>A	ENSP00000357981.3:p.Arg311=
ENST00000448301.6:c.781C>A	ENSP00000408414.1:p.Arg261=
ENST00000472977.6:c.224C>A
ENST00000483930.1:c.479C>A	ENSP00000475812.1:n.479C>A
NM_001199739.1:c.781C>A	NP_001186668.1:p.Arg261=
NM_004079.4:c.931C>A	NP_004070.3:p.Arg311=
NM_004079.5:c.931C>A MANE Select	NP_004070.3:p.Arg311=
NM_001199739.2:c.781C>A	NP_001186668.1:p.Arg261=