Canonical Allele Identifier: CA342322371

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705560A>C (hg19) ; chr1:g.150733084A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733084A>C , CM000663.2:g.150733084A>C	GRCh38
NC_000001.10:g.150705560A>C , CM000663.1:g.150705560A>C	GRCh37
NC_000001.9:g.148972184A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.958T>G MANE Select	ENSP00000357981.3:p.Cys320Gly
ENST00000448301.7:c.730T>G	ENSP00000408414.2:p.Cys244Gly
ENST00000472977.7:c.958T>G	ENSP00000475176.2:p.Cys320Gly
ENST00000483930.2:c.*152T>G	ENSP00000475812.2:n.*152T>G
ENST00000607427.2:c.958T>G	ENSP00000475557.2:p.Cys320Gly
ENST00000679512.1:c.855T>G	ENSP00000505113.1:p.Ile285Met
ENST00000679898.1:c.685T>G	ENSP00000505326.1:p.Cys229Gly
ENST00000680288.1:c.808T>G	ENSP00000506001.1:p.Cys270Gly
ENST00000680311.1:c.*41T>G	ENSP00000505020.1:n.*41T>G
ENST00000680471.1:c.*129T>G	ENSP00000506603.1:n.*129T>G
ENST00000680664.1:c.781T>G	ENSP00000506248.1:p.Cys261Gly
ENST00000680931.1:c.*308T>G	ENSP00000504934.1:n.*308T>G
ENST00000681357.1:n.348T>G
ENST00000681444.1:c.958T>G	ENSP00000505359.1:p.Cys320Gly
ENST00000368985.7:c.958T>G	ENSP00000357981.3:p.Cys320Gly
ENST00000448301.6:c.808T>G	ENSP00000408414.1:p.Cys270Gly
ENST00000472977.6:c.251T>G
ENST00000483930.1:c.506T>G	ENSP00000475812.1:n.506T>G
NM_001199739.1:c.808T>G	NP_001186668.1:p.Cys270Gly
NM_004079.4:c.958T>G	NP_004070.3:p.Cys320Gly
NM_004079.5:c.958T>G MANE Select	NP_004070.3:p.Cys320Gly
NM_001199739.2:c.808T>G	NP_001186668.1:p.Cys270Gly