Canonical Allele Identifier: CA342322372

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705561A>C (hg19) ; chr1:g.150733085A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733085A>C , CM000663.2:g.150733085A>C	GRCh38
NC_000001.10:g.150705561A>C , CM000663.1:g.150705561A>C	GRCh37
NC_000001.9:g.148972185A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.957T>G MANE Select	ENSP00000357981.3:p.His319Gln
ENST00000448301.7:c.729T>G	ENSP00000408414.2:p.His243Gln
ENST00000472977.7:c.957T>G	ENSP00000475176.2:p.His319Gln
ENST00000483930.2:c.*151T>G	ENSP00000475812.2:n.*151T>G
ENST00000607427.2:c.957T>G	ENSP00000475557.2:p.His319Gln
ENST00000679512.1:c.854T>G	ENSP00000505113.1:p.Ile285Ser
ENST00000679898.1:c.684T>G	ENSP00000505326.1:p.His228Gln
ENST00000680288.1:c.807T>G	ENSP00000506001.1:p.His269Gln
ENST00000680311.1:c.*40T>G	ENSP00000505020.1:n.*40T>G
ENST00000680471.1:c.*128T>G	ENSP00000506603.1:n.*128T>G
ENST00000680664.1:c.780T>G	ENSP00000506248.1:p.His260Gln
ENST00000680931.1:c.*307T>G	ENSP00000504934.1:n.*307T>G
ENST00000681357.1:n.347T>G
ENST00000681444.1:c.957T>G	ENSP00000505359.1:p.His319Gln
ENST00000368985.7:c.957T>G	ENSP00000357981.3:p.His319Gln
ENST00000448301.6:c.807T>G	ENSP00000408414.1:p.His269Gln
ENST00000472977.6:c.250T>G
ENST00000483930.1:c.505T>G	ENSP00000475812.1:n.505T>G
NM_001199739.1:c.807T>G	NP_001186668.1:p.His269Gln
NM_004079.4:c.957T>G	NP_004070.3:p.His319Gln
NM_004079.5:c.957T>G MANE Select	NP_004070.3:p.His319Gln
NM_001199739.2:c.807T>G	NP_001186668.1:p.His269Gln