Canonical Allele Identifier: CA342322299

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705529T>C (hg19) ; chr1:g.150733053T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733053T>C , CM000663.2:g.150733053T>C	GRCh38
NC_000001.10:g.150705529T>C , CM000663.1:g.150705529T>C	GRCh37
NC_000001.9:g.148972153T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.989A>G MANE Select	ENSP00000357981.3:p.Glu330Gly
ENST00000448301.7:c.761A>G	ENSP00000408414.2:p.Glu254Gly
ENST00000472977.7:c.989A>G	ENSP00000475176.2:p.Glu330Gly
ENST00000483930.2:c.*183A>G	ENSP00000475812.2:n.*183A>G
ENST00000607427.2:c.989A>G	ENSP00000475557.2:p.Glu330Gly
ENST00000679512.1:c.886A>G	ENSP00000505113.1:p.Lys296Glu
ENST00000679898.1:c.716A>G	ENSP00000505326.1:p.Glu239Gly
ENST00000680288.1:c.839A>G	ENSP00000506001.1:p.Glu280Gly
ENST00000680311.1:c.*72A>G	ENSP00000505020.1:n.*72A>G
ENST00000680471.1:c.*160A>G	ENSP00000506603.1:n.*160A>G
ENST00000680664.1:c.812A>G	ENSP00000506248.1:p.Glu271Gly
ENST00000680931.1:c.*339A>G	ENSP00000504934.1:n.*339A>G
ENST00000681357.1:n.379A>G
ENST00000681444.1:c.989A>G	ENSP00000505359.1:p.Glu330Gly
ENST00000368985.7:c.989A>G	ENSP00000357981.3:p.Glu330Gly
ENST00000448301.6:c.839A>G	ENSP00000408414.1:p.Glu280Gly
ENST00000472977.6:c.282A>G
ENST00000483930.1:c.537A>G	ENSP00000475812.1:n.537A>G
ENST00000607427.1:c.10A>G
NM_001199739.1:c.839A>G	NP_001186668.1:p.Glu280Gly
NM_004079.4:c.989A>G	NP_004070.3:p.Glu330Gly
NM_004079.5:c.989A>G MANE Select	NP_004070.3:p.Glu330Gly
NM_001199739.2:c.839A>G	NP_001186668.1:p.Glu280Gly