Canonical Allele Identifier: CA342336739

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776687C>G (hg19) ; chr1:g.150804211C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804211C>G , CM000663.2:g.150804211C>G	GRCh38
NC_000001.10:g.150776687C>G , CM000663.1:g.150776687C>G	GRCh37
NC_000001.9:g.149043311C>G	NCBI36
NG_011848.1:g.9126G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.428G>C MANE Select	ENSP00000271651.3:p.Ser143Thr
ENST00000443913.2:c.605G>C	ENSP00000405083.2:p.Ser202Thr
ENST00000480670.2:n.3497G>C
ENST00000676680.1:c.428G>C	ENSP00000503270.1:p.Ser143Thr
ENST00000676716.1:c.305G>C	ENSP00000504737.1:p.Ser102Thr
ENST00000676751.1:c.428G>C	ENSP00000502964.1:p.Ser143Thr
ENST00000676824.1:c.428G>C	ENSP00000504176.1:p.Ser143Thr
ENST00000676966.1:c.428G>C	ENSP00000503723.1:p.Ser143Thr
ENST00000676970.1:c.428G>C	ENSP00000503832.1:p.Ser143Thr
ENST00000677330.1:n.2254G>C
ENST00000677611.1:n.280G>C
ENST00000677887.1:c.470G>C	ENSP00000503876.1:p.Ser157Thr
ENST00000678275.1:c.*320G>C	ENSP00000504796.1:n.*320G>C
ENST00000678337.1:c.464G>C	ENSP00000504759.1:p.Ser155Thr
ENST00000678725.1:n.1405G>C
ENST00000679090.1:n.1013G>C
ENST00000679148.1:n.3390G>C
ENST00000679171.1:n.2789G>C
ENST00000679260.1:c.399+1650G>C	ENSP00000504534.1:n.399+1650G>C
ENST00000271651.7:c.428G>C	ENSP00000271651.3:p.Ser143Thr
ENST00000443913.1:c.605G>C	ENSP00000405083.1:p.Ser202Thr
ENST00000480670.1:n.268G>C
NM_000396.3:c.428G>C	NP_000387.1:p.Ser143Thr
NM_000396.4:c.428G>C MANE Select	NP_000387.1:p.Ser143Thr