Canonical Allele Identifier: CA30094948

Gene: CTSS

Linked Data

• dbSNP Id: rs866627817
• MyVariant Identifiers: chr1:g.150705497A>G (hg19) ; chr1:g.150733021A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733021A>G , CM000663.2:g.150733021A>G	GRCh38
NC_000001.10:g.150705497A>G , CM000663.1:g.150705497A>G	GRCh37
NC_000001.9:g.148972121A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.*25T>C MANE Select	ENSP00000357981.3:n.*25T>C
ENST00000448301.7:c.*25T>C	ENSP00000408414.2:n.*25T>C
ENST00000472977.7:c.*25T>C	ENSP00000475176.2:n.*25T>C
ENST00000483930.2:c.*215T>C	ENSP00000475812.2:n.*215T>C
ENST00000607427.2:c.*25T>C	ENSP00000475557.2:n.*25T>C
ENST00000679512.1:c.918T>C	ENSP00000505113.1:p.Asn306=
ENST00000679898.1:c.*25T>C	ENSP00000505326.1:n.*25T>C
ENST00000680288.1:c.*25T>C	ENSP00000506001.1:n.*25T>C
ENST00000680311.1:c.*104T>C	ENSP00000505020.1:n.*104T>C
ENST00000680471.1:c.*192T>C	ENSP00000506603.1:n.*192T>C
ENST00000680664.1:c.*25T>C	ENSP00000506248.1:n.*25T>C
ENST00000680931.1:c.*371T>C	ENSP00000504934.1:n.*371T>C
ENST00000681357.1:n.411T>C
ENST00000681444.1:c.*25T>C	ENSP00000505359.1:n.*25T>C
ENST00000368985.7:c.*25T>C	ENSP00000357981.3:n.*25T>C
ENST00000448301.6:c.*25T>C	ENSP00000408414.1:n.*25T>C
ENST00000472977.6:c.314T>C
ENST00000483930.1:c.569T>C	ENSP00000475812.1:n.569T>C
ENST00000607427.1:c.42T>C
NM_001199739.1:c.*25T>C	NP_001186668.1:n.*25T>C
NM_004079.4:c.*25T>C	NP_004070.3:n.*25T>C
NM_004079.5:c.*25T>C MANE Select	NP_004070.3:n.*25T>C
NM_001199739.2:c.*25T>C	NP_001186668.1:n.*25T>C