Canonical Allele Identifier: CA342322492

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705612G>C (hg19) ; chr1:g.150733136G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733136G>C , CM000663.2:g.150733136G>C	GRCh38
NC_000001.10:g.150705612G>C , CM000663.1:g.150705612G>C	GRCh37
NC_000001.9:g.148972236G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.906C>G MANE Select	ENSP00000357981.3:p.His302Gln
ENST00000448301.7:c.678C>G	ENSP00000408414.2:p.His226Gln
ENST00000472977.7:c.906C>G	ENSP00000475176.2:p.His302Gln
ENST00000483930.2:c.*100C>G	ENSP00000475812.2:n.*100C>G
ENST00000607427.2:c.906C>G	ENSP00000475557.2:p.His302Gln
ENST00000679512.1:c.803C>G	ENSP00000505113.1:p.Thr268Arg
ENST00000679898.1:c.633C>G	ENSP00000505326.1:p.His211Gln
ENST00000680288.1:c.756C>G	ENSP00000506001.1:p.His252Gln
ENST00000680311.1:c.637C>G	ENSP00000505020.1:p.Gln213Glu
ENST00000680471.1:c.*77C>G	ENSP00000506603.1:n.*77C>G
ENST00000680664.1:c.729C>G	ENSP00000506248.1:p.His243Gln
ENST00000680931.1:c.*256C>G	ENSP00000504934.1:n.*256C>G
ENST00000681357.1:n.296C>G
ENST00000681444.1:c.906C>G	ENSP00000505359.1:p.His302Gln
ENST00000368985.7:c.906C>G	ENSP00000357981.3:p.His302Gln
ENST00000448301.6:c.756C>G	ENSP00000408414.1:p.His252Gln
ENST00000472977.6:c.199C>G
ENST00000483930.1:c.454C>G	ENSP00000475812.1:n.454C>G
NM_001199739.1:c.756C>G	NP_001186668.1:p.His252Gln
NM_004079.4:c.906C>G	NP_004070.3:p.His302Gln
NM_004079.5:c.906C>G MANE Select	NP_004070.3:p.His302Gln
NM_001199739.2:c.756C>G	NP_001186668.1:p.His252Gln