Canonical Allele Identifier: CA342322290

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705526A>C (hg19) ; chr1:g.150733050A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733050A>C , CM000663.2:g.150733050A>C	GRCh38
NC_000001.10:g.150705526A>C , CM000663.1:g.150705526A>C	GRCh37
NC_000001.9:g.148972150A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.992T>G MANE Select	ENSP00000357981.3:p.Ile331Ser
ENST00000448301.7:c.764T>G	ENSP00000408414.2:p.Ile255Ser
ENST00000472977.7:c.992T>G	ENSP00000475176.2:p.Ile331Ser
ENST00000483930.2:c.*186T>G	ENSP00000475812.2:n.*186T>G
ENST00000607427.2:c.992T>G	ENSP00000475557.2:p.Ile331Ser
ENST00000679512.1:c.889T>G	ENSP00000505113.1:p.Ser297Ala
ENST00000679898.1:c.719T>G	ENSP00000505326.1:p.Ile240Ser
ENST00000680288.1:c.842T>G	ENSP00000506001.1:p.Ile281Ser
ENST00000680311.1:c.*75T>G	ENSP00000505020.1:n.*75T>G
ENST00000680471.1:c.*163T>G	ENSP00000506603.1:n.*163T>G
ENST00000680664.1:c.815T>G	ENSP00000506248.1:p.Ile272Ser
ENST00000680931.1:c.*342T>G	ENSP00000504934.1:n.*342T>G
ENST00000681357.1:n.382T>G
ENST00000681444.1:c.992T>G	ENSP00000505359.1:p.Ile331Ser
ENST00000368985.7:c.992T>G	ENSP00000357981.3:p.Ile331Ser
ENST00000448301.6:c.842T>G	ENSP00000408414.1:p.Ile281Ser
ENST00000472977.6:c.285T>G
ENST00000483930.1:c.540T>G	ENSP00000475812.1:n.540T>G
ENST00000607427.1:c.13T>G
NM_001199739.1:c.842T>G	NP_001186668.1:p.Ile281Ser
NM_004079.4:c.992T>G	NP_004070.3:p.Ile331Ser
NM_004079.5:c.992T>G MANE Select	NP_004070.3:p.Ile331Ser
NM_001199739.2:c.842T>G	NP_001186668.1:p.Ile281Ser