Canonical Allele Identifier: CA342322428

Gene: CTSS

Linked Data

• dbSNP Id: rs1652558721
• MyVariant Identifiers: chr1:g.150705583A>T (hg19) ; chr1:g.150733107A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733107A>T , CM000663.2:g.150733107A>T	GRCh38
NC_000001.10:g.150705583A>T , CM000663.1:g.150705583A>T	GRCh37
NC_000001.9:g.148972207A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.935T>A MANE Select	ENSP00000357981.3:p.Met312Lys
ENST00000448301.7:c.707T>A	ENSP00000408414.2:p.Met236Lys
ENST00000472977.7:c.935T>A	ENSP00000475176.2:p.Met312Lys
ENST00000483930.2:c.*129T>A	ENSP00000475812.2:n.*129T>A
ENST00000607427.2:c.935T>A	ENSP00000475557.2:p.Met312Lys
ENST00000679512.1:c.832T>A	ENSP00000505113.1:p.Trp278Arg
ENST00000679898.1:c.662T>A	ENSP00000505326.1:p.Met221Lys
ENST00000680288.1:c.785T>A	ENSP00000506001.1:p.Met262Lys
ENST00000680311.1:c.*18T>A	ENSP00000505020.1:n.*18T>A
ENST00000680471.1:c.*106T>A	ENSP00000506603.1:n.*106T>A
ENST00000680664.1:c.758T>A	ENSP00000506248.1:p.Met253Lys
ENST00000680931.1:c.*285T>A	ENSP00000504934.1:n.*285T>A
ENST00000681357.1:n.325T>A
ENST00000681444.1:c.935T>A	ENSP00000505359.1:p.Met312Lys
ENST00000368985.7:c.935T>A	ENSP00000357981.3:p.Met312Lys
ENST00000448301.6:c.785T>A	ENSP00000408414.1:p.Met262Lys
ENST00000472977.6:c.228T>A
ENST00000483930.1:c.483T>A	ENSP00000475812.1:n.483T>A
NM_001199739.1:c.785T>A	NP_001186668.1:p.Met262Lys
NM_004079.4:c.935T>A	NP_004070.3:p.Met312Lys
NM_004079.5:c.935T>A MANE Select	NP_004070.3:p.Met312Lys
NM_001199739.2:c.785T>A	NP_001186668.1:p.Met262Lys