Canonical Allele Identifier: CA342322284

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705523T>C (hg19) ; chr1:g.150733047T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733047T>C , CM000663.2:g.150733047T>C	GRCh38
NC_000001.10:g.150705523T>C , CM000663.1:g.150705523T>C	GRCh37
NC_000001.9:g.148972147T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.995A>G MANE Select	ENSP00000357981.3:p.Ter332Trp
ENST00000448301.7:c.767A>G	ENSP00000408414.2:p.Ter256Trp
ENST00000472977.7:c.995A>G	ENSP00000475176.2:p.Ter332Trp
ENST00000483930.2:c.*189A>G	ENSP00000475812.2:n.*189A>G
ENST00000607427.2:c.995A>G	ENSP00000475557.2:p.Ter332Trp
ENST00000679512.1:c.892A>G	ENSP00000505113.1:p.Arg298Gly
ENST00000679898.1:c.722A>G	ENSP00000505326.1:p.Ter241Trp
ENST00000680288.1:c.845A>G	ENSP00000506001.1:p.Ter282Trp
ENST00000680311.1:c.*78A>G	ENSP00000505020.1:n.*78A>G
ENST00000680471.1:c.*166A>G	ENSP00000506603.1:n.*166A>G
ENST00000680664.1:c.818A>G	ENSP00000506248.1:p.Ter273Trp
ENST00000680931.1:c.*345A>G	ENSP00000504934.1:n.*345A>G
ENST00000681357.1:n.385A>G
ENST00000681444.1:c.995A>G	ENSP00000505359.1:p.Ter332Trp
ENST00000368985.7:c.995A>G	ENSP00000357981.3:p.Ter332Trp
ENST00000448301.6:c.845A>G	ENSP00000408414.1:p.Ter282Trp
ENST00000472977.6:c.288A>G
ENST00000483930.1:c.543A>G	ENSP00000475812.1:n.543A>G
ENST00000607427.1:c.16A>G
NM_001199739.1:c.845A>G	NP_001186668.1:p.Ter282Trp
NM_004079.4:c.995A>G	NP_004070.3:p.Ter332Trp
NM_004079.5:c.995A>G MANE Select	NP_004070.3:p.Ter332Trp
NM_001199739.2:c.845A>G	NP_001186668.1:p.Ter282Trp