Canonical Allele Identifier: CA342322447

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705593A>C (hg19) ; chr1:g.150733117A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733117A>C , CM000663.2:g.150733117A>C	GRCh38
NC_000001.10:g.150705593A>C , CM000663.1:g.150705593A>C	GRCh37
NC_000001.9:g.148972217A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.925T>G MANE Select	ENSP00000357981.3:p.Tyr309Asp
ENST00000448301.7:c.697T>G	ENSP00000408414.2:p.Tyr233Asp
ENST00000472977.7:c.925T>G	ENSP00000475176.2:p.Tyr309Asp
ENST00000483930.2:c.*119T>G	ENSP00000475812.2:n.*119T>G
ENST00000607427.2:c.925T>G	ENSP00000475557.2:p.Tyr309Asp
ENST00000679512.1:c.822T>G	ENSP00000505113.1:p.Asp274Glu
ENST00000679898.1:c.652T>G	ENSP00000505326.1:p.Tyr218Asp
ENST00000680288.1:c.775T>G	ENSP00000506001.1:p.Tyr259Asp
ENST00000680311.1:c.*8T>G	ENSP00000505020.1:n.*8T>G
ENST00000680471.1:c.*96T>G	ENSP00000506603.1:n.*96T>G
ENST00000680664.1:c.748T>G	ENSP00000506248.1:p.Tyr250Asp
ENST00000680931.1:c.*275T>G	ENSP00000504934.1:n.*275T>G
ENST00000681357.1:n.315T>G
ENST00000681444.1:c.925T>G	ENSP00000505359.1:p.Tyr309Asp
ENST00000368985.7:c.925T>G	ENSP00000357981.3:p.Tyr309Asp
ENST00000448301.6:c.775T>G	ENSP00000408414.1:p.Tyr259Asp
ENST00000472977.6:c.218T>G
ENST00000483930.1:c.473T>G	ENSP00000475812.1:n.473T>G
NM_001199739.1:c.775T>G	NP_001186668.1:p.Tyr259Asp
NM_004079.4:c.925T>G	NP_004070.3:p.Tyr309Asp
NM_004079.5:c.925T>G MANE Select	NP_004070.3:p.Tyr309Asp
NM_001199739.2:c.775T>G	NP_001186668.1:p.Tyr259Asp