Canonical Allele Identifier: CA342322504

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705617C>A (hg19) ; chr1:g.150733141C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733141C>A , CM000663.2:g.150733141C>A	GRCh38
NC_000001.10:g.150705617C>A , CM000663.1:g.150705617C>A	GRCh37
NC_000001.9:g.148972241C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.901G>T MANE Select	ENSP00000357981.3:p.Gly301Cys
ENST00000448301.7:c.673G>T	ENSP00000408414.2:p.Gly225Cys
ENST00000472977.7:c.901G>T	ENSP00000475176.2:p.Gly301Cys
ENST00000483930.2:c.*95G>T	ENSP00000475812.2:n.*95G>T
ENST00000607427.2:c.901G>T	ENSP00000475557.2:p.Gly301Cys
ENST00000679512.1:c.798G>T	ENSP00000505113.1:p.Gly266=
ENST00000679898.1:c.628G>T	ENSP00000505326.1:p.Gly210Cys
ENST00000680288.1:c.751G>T	ENSP00000506001.1:p.Gly251Cys
ENST00000680311.1:c.632G>T	ENSP00000505020.1:p.Gly211Val
ENST00000680471.1:c.*72G>T	ENSP00000506603.1:n.*72G>T
ENST00000680664.1:c.724G>T	ENSP00000506248.1:p.Gly242Cys
ENST00000680931.1:c.*251G>T	ENSP00000504934.1:n.*251G>T
ENST00000681357.1:n.291G>T
ENST00000681444.1:c.901G>T	ENSP00000505359.1:p.Gly301Cys
ENST00000368985.7:c.901G>T	ENSP00000357981.3:p.Gly301Cys
ENST00000448301.6:c.751G>T	ENSP00000408414.1:p.Gly251Cys
ENST00000472977.6:c.194G>T
ENST00000483930.1:c.449G>T	ENSP00000475812.1:n.449G>T
NM_001199739.1:c.751G>T	NP_001186668.1:p.Gly251Cys
NM_004079.4:c.901G>T	NP_004070.3:p.Gly301Cys
NM_004079.5:c.901G>T MANE Select	NP_004070.3:p.Gly301Cys
NM_001199739.2:c.751G>T	NP_001186668.1:p.Gly251Cys