Canonical Allele Identifier: CA342322467

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705601T>C (hg19) ; chr1:g.150733125T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733125T>C , CM000663.2:g.150733125T>C	GRCh38
NC_000001.10:g.150705601T>C , CM000663.1:g.150705601T>C	GRCh37
NC_000001.9:g.148972225T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.917A>G MANE Select	ENSP00000357981.3:p.Glu306Gly
ENST00000448301.7:c.689A>G	ENSP00000408414.2:p.Glu230Gly
ENST00000472977.7:c.917A>G	ENSP00000475176.2:p.Glu306Gly
ENST00000483930.2:c.*111A>G	ENSP00000475812.2:n.*111A>G
ENST00000607427.2:c.917A>G	ENSP00000475557.2:p.Glu306Gly
ENST00000679512.1:c.814A>G	ENSP00000505113.1:p.Lys272Glu
ENST00000679898.1:c.644A>G	ENSP00000505326.1:p.Glu215Gly
ENST00000680288.1:c.767A>G	ENSP00000506001.1:p.Glu256Gly
ENST00000680311.1:c.648A>G	ENSP00000505020.1:p.Ter216Trp
ENST00000680471.1:c.*88A>G	ENSP00000506603.1:n.*88A>G
ENST00000680664.1:c.740A>G	ENSP00000506248.1:p.Glu247Gly
ENST00000680931.1:c.*267A>G	ENSP00000504934.1:n.*267A>G
ENST00000681357.1:n.307A>G
ENST00000681444.1:c.917A>G	ENSP00000505359.1:p.Glu306Gly
ENST00000368985.7:c.917A>G	ENSP00000357981.3:p.Glu306Gly
ENST00000448301.6:c.767A>G	ENSP00000408414.1:p.Glu256Gly
ENST00000472977.6:c.210A>G
ENST00000483930.1:c.465A>G	ENSP00000475812.1:n.465A>G
NM_001199739.1:c.767A>G	NP_001186668.1:p.Glu256Gly
NM_004079.4:c.917A>G	NP_004070.3:p.Glu306Gly
NM_004079.5:c.917A>G MANE Select	NP_004070.3:p.Glu306Gly
NM_001199739.2:c.767A>G	NP_001186668.1:p.Glu256Gly