Canonical Allele Identifier: CA342336443

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776552T>G (hg19) ; chr1:g.150804076T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804076T>G , CM000663.2:g.150804076T>G	GRCh38
NC_000001.10:g.150776552T>G , CM000663.1:g.150776552T>G	GRCh37
NC_000001.9:g.149043176T>G	NCBI36
NG_011848.1:g.9261A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.563A>C MANE Select	ENSP00000271651.3:p.Tyr188Ser
ENST00000443913.2:c.740A>C	ENSP00000405083.2:p.Tyr247Ser
ENST00000480670.2:n.3632A>C
ENST00000676680.1:c.563A>C	ENSP00000503270.1:p.Tyr188Ser
ENST00000676716.1:c.440A>C	ENSP00000504737.1:p.Tyr147Ser
ENST00000676751.1:c.563A>C	ENSP00000502964.1:p.Tyr188Ser
ENST00000676824.1:c.563A>C	ENSP00000504176.1:p.Tyr188Ser
ENST00000676966.1:c.563A>C	ENSP00000503723.1:p.Tyr188Ser
ENST00000676970.1:c.563A>C	ENSP00000503832.1:p.Tyr188Ser
ENST00000677330.1:n.2389A>C
ENST00000677611.1:n.415A>C
ENST00000677887.1:c.605A>C	ENSP00000503876.1:p.Tyr202Ser
ENST00000678275.1:c.*455A>C	ENSP00000504796.1:n.*455A>C
ENST00000678337.1:c.599A>C	ENSP00000504759.1:p.Tyr200Ser
ENST00000678725.1:n.1540A>C
ENST00000679090.1:n.1148A>C
ENST00000679148.1:n.3525A>C
ENST00000679171.1:n.2924A>C
ENST00000679260.1:c.399+1785A>C	ENSP00000504534.1:n.399+1785A>C
ENST00000271651.7:c.563A>C	ENSP00000271651.3:p.Tyr188Ser
ENST00000443913.1:c.740A>C	ENSP00000405083.1:p.Tyr247Ser
ENST00000480670.1:n.403A>C
NM_000396.3:c.563A>C	NP_000387.1:p.Tyr188Ser
NM_000396.4:c.563A>C MANE Select	NP_000387.1:p.Tyr188Ser