Canonical Allele Identifier: CA342322443

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705591A>T (hg19) ; chr1:g.150733115A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733115A>T , CM000663.2:g.150733115A>T	GRCh38
NC_000001.10:g.150705591A>T , CM000663.1:g.150705591A>T	GRCh37
NC_000001.9:g.148972215A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.927T>A MANE Select	ENSP00000357981.3:p.Tyr309Ter
ENST00000448301.7:c.699T>A	ENSP00000408414.2:p.Tyr233Ter
ENST00000472977.7:c.927T>A	ENSP00000475176.2:p.Tyr309Ter
ENST00000483930.2:c.*121T>A	ENSP00000475812.2:n.*121T>A
ENST00000607427.2:c.927T>A	ENSP00000475557.2:p.Tyr309Ter
ENST00000679512.1:c.824T>A	ENSP00000505113.1:p.Ile275Lys
ENST00000679898.1:c.654T>A	ENSP00000505326.1:p.Tyr218Ter
ENST00000680288.1:c.777T>A	ENSP00000506001.1:p.Tyr259Ter
ENST00000680311.1:c.*10T>A	ENSP00000505020.1:n.*10T>A
ENST00000680471.1:c.*98T>A	ENSP00000506603.1:n.*98T>A
ENST00000680664.1:c.750T>A	ENSP00000506248.1:p.Tyr250Ter
ENST00000680931.1:c.*277T>A	ENSP00000504934.1:n.*277T>A
ENST00000681357.1:n.317T>A
ENST00000681444.1:c.927T>A	ENSP00000505359.1:p.Tyr309Ter
ENST00000368985.7:c.927T>A	ENSP00000357981.3:p.Tyr309Ter
ENST00000448301.6:c.777T>A	ENSP00000408414.1:p.Tyr259Ter
ENST00000472977.6:c.220T>A
ENST00000483930.1:c.475T>A	ENSP00000475812.1:n.475T>A
NM_001199739.1:c.777T>A	NP_001186668.1:p.Tyr259Ter
NM_004079.4:c.927T>A	NP_004070.3:p.Tyr309Ter
NM_004079.5:c.927T>A MANE Select	NP_004070.3:p.Tyr309Ter
NM_001199739.2:c.777T>A	NP_001186668.1:p.Tyr259Ter