Canonical Allele Identifier: CA342322430

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705584T>C (hg19) ; chr1:g.150733108T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733108T>C , CM000663.2:g.150733108T>C	GRCh38
NC_000001.10:g.150705584T>C , CM000663.1:g.150705584T>C	GRCh37
NC_000001.9:g.148972208T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.934A>G MANE Select	ENSP00000357981.3:p.Met312Val
ENST00000448301.7:c.706A>G	ENSP00000408414.2:p.Met236Val
ENST00000472977.7:c.934A>G	ENSP00000475176.2:p.Met312Val
ENST00000483930.2:c.*128A>G	ENSP00000475812.2:n.*128A>G
ENST00000607427.2:c.934A>G	ENSP00000475557.2:p.Met312Val
ENST00000679512.1:c.831A>G	ENSP00000505113.1:p.Gly277=
ENST00000679898.1:c.661A>G	ENSP00000505326.1:p.Met221Val
ENST00000680288.1:c.784A>G	ENSP00000506001.1:p.Met262Val
ENST00000680311.1:c.*17A>G	ENSP00000505020.1:n.*17A>G
ENST00000680471.1:c.*105A>G	ENSP00000506603.1:n.*105A>G
ENST00000680664.1:c.757A>G	ENSP00000506248.1:p.Met253Val
ENST00000680931.1:c.*284A>G	ENSP00000504934.1:n.*284A>G
ENST00000681357.1:n.324A>G
ENST00000681444.1:c.934A>G	ENSP00000505359.1:p.Met312Val
ENST00000368985.7:c.934A>G	ENSP00000357981.3:p.Met312Val
ENST00000448301.6:c.784A>G	ENSP00000408414.1:p.Met262Val
ENST00000472977.6:c.227A>G
ENST00000483930.1:c.482A>G	ENSP00000475812.1:n.482A>G
NM_001199739.1:c.784A>G	NP_001186668.1:p.Met262Val
NM_004079.4:c.934A>G	NP_004070.3:p.Met312Val
NM_004079.5:c.934A>G MANE Select	NP_004070.3:p.Met312Val
NM_001199739.2:c.784A>G	NP_001186668.1:p.Met262Val