Canonical Allele Identifier: CA342322288

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705524A>T (hg19) ; chr1:g.150733048A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733048A>T , CM000663.2:g.150733048A>T	GRCh38
NC_000001.10:g.150705524A>T , CM000663.1:g.150705524A>T	GRCh37
NC_000001.9:g.148972148A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.994T>A MANE Select	ENSP00000357981.3:p.Ter332Lys
ENST00000448301.7:c.766T>A	ENSP00000408414.2:p.Ter256Lys
ENST00000472977.7:c.994T>A	ENSP00000475176.2:p.Ter332Lys
ENST00000483930.2:c.*188T>A	ENSP00000475812.2:n.*188T>A
ENST00000607427.2:c.994T>A	ENSP00000475557.2:p.Ter332Lys
ENST00000679512.1:c.891T>A	ENSP00000505113.1:p.Ser297=
ENST00000679898.1:c.721T>A	ENSP00000505326.1:p.Ter241Lys
ENST00000680288.1:c.844T>A	ENSP00000506001.1:p.Ter282Lys
ENST00000680311.1:c.*77T>A	ENSP00000505020.1:n.*77T>A
ENST00000680471.1:c.*165T>A	ENSP00000506603.1:n.*165T>A
ENST00000680664.1:c.817T>A	ENSP00000506248.1:p.Ter273Lys
ENST00000680931.1:c.*344T>A	ENSP00000504934.1:n.*344T>A
ENST00000681357.1:n.384T>A
ENST00000681444.1:c.994T>A	ENSP00000505359.1:p.Ter332Lys
ENST00000368985.7:c.994T>A	ENSP00000357981.3:p.Ter332Lys
ENST00000448301.6:c.844T>A	ENSP00000408414.1:p.Ter282Lys
ENST00000472977.6:c.287T>A
ENST00000483930.1:c.542T>A	ENSP00000475812.1:n.542T>A
ENST00000607427.1:c.15T>A
NM_001199739.1:c.844T>A	NP_001186668.1:p.Ter282Lys
NM_004079.4:c.994T>A	NP_004070.3:p.Ter332Lys
NM_004079.5:c.994T>A MANE Select	NP_004070.3:p.Ter332Lys
NM_001199739.2:c.844T>A	NP_001186668.1:p.Ter282Lys