Canonical Allele Identifier: CA342322378

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705563G>C (hg19) ; chr1:g.150733087G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733087G>C , CM000663.2:g.150733087G>C	GRCh38
NC_000001.10:g.150705563G>C , CM000663.1:g.150705563G>C	GRCh37
NC_000001.9:g.148972187G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.955C>G MANE Select	ENSP00000357981.3:p.His319Asp
ENST00000448301.7:c.727C>G	ENSP00000408414.2:p.His243Asp
ENST00000472977.7:c.955C>G	ENSP00000475176.2:p.His319Asp
ENST00000483930.2:c.*149C>G	ENSP00000475812.2:n.*149C>G
ENST00000607427.2:c.955C>G	ENSP00000475557.2:p.His319Asp
ENST00000679512.1:c.852C>G	ENSP00000505113.1:p.Ile284Met
ENST00000679898.1:c.682C>G	ENSP00000505326.1:p.His228Asp
ENST00000680288.1:c.805C>G	ENSP00000506001.1:p.His269Asp
ENST00000680311.1:c.*38C>G	ENSP00000505020.1:n.*38C>G
ENST00000680471.1:c.*126C>G	ENSP00000506603.1:n.*126C>G
ENST00000680664.1:c.778C>G	ENSP00000506248.1:p.His260Asp
ENST00000680931.1:c.*305C>G	ENSP00000504934.1:n.*305C>G
ENST00000681357.1:n.345C>G
ENST00000681444.1:c.955C>G	ENSP00000505359.1:p.His319Asp
ENST00000368985.7:c.955C>G	ENSP00000357981.3:p.His319Asp
ENST00000448301.6:c.805C>G	ENSP00000408414.1:p.His269Asp
ENST00000472977.6:c.248C>G
ENST00000483930.1:c.503C>G	ENSP00000475812.1:n.503C>G
NM_001199739.1:c.805C>G	NP_001186668.1:p.His269Asp
NM_004079.4:c.955C>G	NP_004070.3:p.His319Asp
NM_004079.5:c.955C>G MANE Select	NP_004070.3:p.His319Asp
NM_001199739.2:c.805C>G	NP_001186668.1:p.His269Asp