Canonical Allele Identifier: CA342322434

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705587G>C (hg19) ; chr1:g.150733111G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733111G>C , CM000663.2:g.150733111G>C	GRCh38
NC_000001.10:g.150705587G>C , CM000663.1:g.150705587G>C	GRCh37
NC_000001.9:g.148972211G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.931C>G MANE Select	ENSP00000357981.3:p.Arg311Gly
ENST00000448301.7:c.703C>G	ENSP00000408414.2:p.Arg235Gly
ENST00000472977.7:c.931C>G	ENSP00000475176.2:p.Arg311Gly
ENST00000483930.2:c.*125C>G	ENSP00000475812.2:n.*125C>G
ENST00000607427.2:c.931C>G	ENSP00000475557.2:p.Arg311Gly
ENST00000679512.1:c.828C>G	ENSP00000505113.1:p.Phe276Leu
ENST00000679898.1:c.658C>G	ENSP00000505326.1:p.Arg220Gly
ENST00000680288.1:c.781C>G	ENSP00000506001.1:p.Arg261Gly
ENST00000680311.1:c.*14C>G	ENSP00000505020.1:n.*14C>G
ENST00000680471.1:c.*102C>G	ENSP00000506603.1:n.*102C>G
ENST00000680664.1:c.754C>G	ENSP00000506248.1:p.Arg252Gly
ENST00000680931.1:c.*281C>G	ENSP00000504934.1:n.*281C>G
ENST00000681357.1:n.321C>G
ENST00000681444.1:c.931C>G	ENSP00000505359.1:p.Arg311Gly
ENST00000368985.7:c.931C>G	ENSP00000357981.3:p.Arg311Gly
ENST00000448301.6:c.781C>G	ENSP00000408414.1:p.Arg261Gly
ENST00000472977.6:c.224C>G
ENST00000483930.1:c.479C>G	ENSP00000475812.1:n.479C>G
NM_001199739.1:c.781C>G	NP_001186668.1:p.Arg261Gly
NM_004079.4:c.931C>G	NP_004070.3:p.Arg311Gly
NM_004079.5:c.931C>G MANE Select	NP_004070.3:p.Arg311Gly
NM_001199739.2:c.781C>G	NP_001186668.1:p.Arg261Gly