Canonical Allele Identifier: CA342322292

Gene: CTSS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.992T>A MANE Select	ENSP00000357981.3:p.Ile331Asn
ENST00000448301.7:c.764T>A	ENSP00000408414.2:p.Ile255Asn
ENST00000472977.7:c.992T>A	ENSP00000475176.2:p.Ile331Asn
ENST00000483930.2:c.*186T>A	ENSP00000475812.2:n.*186T>A
ENST00000607427.2:c.992T>A	ENSP00000475557.2:p.Ile331Asn
ENST00000679512.1:c.889T>A	ENSP00000505113.1:p.Ser297Thr
ENST00000679898.1:c.719T>A	ENSP00000505326.1:p.Ile240Asn
ENST00000680288.1:c.842T>A	ENSP00000506001.1:p.Ile281Asn
ENST00000680311.1:c.*75T>A	ENSP00000505020.1:n.*75T>A
ENST00000680471.1:c.*163T>A	ENSP00000506603.1:n.*163T>A
ENST00000680664.1:c.815T>A	ENSP00000506248.1:p.Ile272Asn
ENST00000680931.1:c.*342T>A	ENSP00000504934.1:n.*342T>A
ENST00000681357.1:n.382T>A
ENST00000681444.1:c.992T>A	ENSP00000505359.1:p.Ile331Asn
ENST00000368985.7:c.992T>A	ENSP00000357981.3:p.Ile331Asn
ENST00000448301.6:c.842T>A	ENSP00000408414.1:p.Ile281Asn
ENST00000472977.6:c.285T>A
ENST00000483930.1:c.540T>A	ENSP00000475812.1:n.540T>A
ENST00000607427.1:c.13T>A
NM_001199739.1:c.842T>A	NP_001186668.1:p.Ile281Asn
NM_004079.4:c.992T>A	NP_004070.3:p.Ile331Asn
NM_004079.5:c.992T>A MANE Select	NP_004070.3:p.Ile331Asn
NM_001199739.2:c.842T>A	NP_001186668.1:p.Ile281Asn