Canonical Allele Identifier: CA342322297

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705528T>G (hg19) ; chr1:g.150733052T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733052T>G , CM000663.2:g.150733052T>G	GRCh38
NC_000001.10:g.150705528T>G , CM000663.1:g.150705528T>G	GRCh37
NC_000001.9:g.148972152T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.990A>C MANE Select	ENSP00000357981.3:p.Glu330Asp
ENST00000448301.7:c.762A>C	ENSP00000408414.2:p.Glu254Asp
ENST00000472977.7:c.990A>C	ENSP00000475176.2:p.Glu330Asp
ENST00000483930.2:c.*184A>C	ENSP00000475812.2:n.*184A>C
ENST00000607427.2:c.990A>C	ENSP00000475557.2:p.Glu330Asp
ENST00000679512.1:c.887A>C	ENSP00000505113.1:p.Lys296Thr
ENST00000679898.1:c.717A>C	ENSP00000505326.1:p.Glu239Asp
ENST00000680288.1:c.840A>C	ENSP00000506001.1:p.Glu280Asp
ENST00000680311.1:c.*73A>C	ENSP00000505020.1:n.*73A>C
ENST00000680471.1:c.*161A>C	ENSP00000506603.1:n.*161A>C
ENST00000680664.1:c.813A>C	ENSP00000506248.1:p.Glu271Asp
ENST00000680931.1:c.*340A>C	ENSP00000504934.1:n.*340A>C
ENST00000681357.1:n.380A>C
ENST00000681444.1:c.990A>C	ENSP00000505359.1:p.Glu330Asp
ENST00000368985.7:c.990A>C	ENSP00000357981.3:p.Glu330Asp
ENST00000448301.6:c.840A>C	ENSP00000408414.1:p.Glu280Asp
ENST00000472977.6:c.283A>C
ENST00000483930.1:c.538A>C	ENSP00000475812.1:n.538A>C
ENST00000607427.1:c.11A>C
NM_001199739.1:c.840A>C	NP_001186668.1:p.Glu280Asp
NM_004079.4:c.990A>C	NP_004070.3:p.Glu330Asp
NM_004079.5:c.990A>C MANE Select	NP_004070.3:p.Glu330Asp
NM_001199739.2:c.840A>C	NP_001186668.1:p.Glu280Asp