Canonical Allele Identifier: CA342322505

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705618C>A (hg19) ; chr1:g.150733142C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733142C>A , CM000663.2:g.150733142C>A	GRCh38
NC_000001.10:g.150705618C>A , CM000663.1:g.150705618C>A	GRCh37
NC_000001.9:g.148972242C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.900G>T MANE Select	ENSP00000357981.3:p.Trp300Cys
ENST00000448301.7:c.672G>T	ENSP00000408414.2:p.Trp224Cys
ENST00000472977.7:c.900G>T	ENSP00000475176.2:p.Trp300Cys
ENST00000483930.2:c.*94G>T	ENSP00000475812.2:n.*94G>T
ENST00000607427.2:c.900G>T	ENSP00000475557.2:p.Trp300Cys
ENST00000679512.1:c.797G>T	ENSP00000505113.1:p.Gly266Val
ENST00000679898.1:c.627G>T	ENSP00000505326.1:p.Trp209Cys
ENST00000680288.1:c.750G>T	ENSP00000506001.1:p.Trp250Cys
ENST00000680311.1:c.631G>T	ENSP00000505020.1:p.Gly211Trp
ENST00000680471.1:c.*71G>T	ENSP00000506603.1:n.*71G>T
ENST00000680664.1:c.723G>T	ENSP00000506248.1:p.Trp241Cys
ENST00000680931.1:c.*250G>T	ENSP00000504934.1:n.*250G>T
ENST00000681357.1:n.290G>T
ENST00000681444.1:c.900G>T	ENSP00000505359.1:p.Trp300Cys
ENST00000368985.7:c.900G>T	ENSP00000357981.3:p.Trp300Cys
ENST00000448301.6:c.750G>T	ENSP00000408414.1:p.Trp250Cys
ENST00000472977.6:c.193G>T
ENST00000483930.1:c.448G>T	ENSP00000475812.1:n.448G>T
NM_001199739.1:c.750G>T	NP_001186668.1:p.Trp250Cys
NM_004079.4:c.900G>T	NP_004070.3:p.Trp300Cys
NM_004079.5:c.900G>T MANE Select	NP_004070.3:p.Trp300Cys
NM_001199739.2:c.750G>T	NP_001186668.1:p.Trp250Cys