Canonical Allele Identifier: CA420699410

Gene: CTSK

Linked Data

• dbSNP Id: rs1654042387
• MyVariant Identifiers: chr1:g.150776566G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804090G>A , CM000663.2:g.150804090G>A	GRCh38
NC_000001.10:g.150776566G>A , CM000663.1:g.150776566G>A	GRCh37
NC_000001.9:g.149043190G>A	NCBI36
NG_011848.1:g.9247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.549C>T MANE Select	ENSP00000271651.3:p.Thr183=
ENST00000443913.2:c.726C>T	ENSP00000405083.2:p.Thr242=
ENST00000480670.2:n.3618C>T
ENST00000676680.1:c.549C>T	ENSP00000503270.1:p.Thr183=
ENST00000676716.1:c.426C>T	ENSP00000504737.1:p.Thr142=
ENST00000676751.1:c.549C>T	ENSP00000502964.1:p.Thr183=
ENST00000676824.1:c.549C>T	ENSP00000504176.1:p.Thr183=
ENST00000676966.1:c.549C>T	ENSP00000503723.1:p.Thr183=
ENST00000676970.1:c.549C>T	ENSP00000503832.1:p.Thr183=
ENST00000677330.1:n.2375C>T
ENST00000677611.1:n.401C>T
ENST00000677887.1:c.591C>T	ENSP00000503876.1:p.Thr197=
ENST00000678275.1:c.*441C>T	ENSP00000504796.1:n.*441C>T
ENST00000678337.1:c.585C>T	ENSP00000504759.1:p.Thr195=
ENST00000678725.1:n.1526C>T
ENST00000679090.1:n.1134C>T
ENST00000679148.1:n.3511C>T
ENST00000679171.1:n.2910C>T
ENST00000679260.1:c.399+1771C>T	ENSP00000504534.1:n.399+1771C>T
ENST00000271651.7:c.549C>T	ENSP00000271651.3:p.Thr183=
ENST00000443913.1:c.726C>T	ENSP00000405083.1:p.Thr242=
ENST00000480670.1:n.389C>T
NM_000396.3:c.549C>T	NP_000387.1:p.Thr183=
NM_000396.4:c.549C>T MANE Select	NP_000387.1:p.Thr183=