Canonical Allele Identifier: CA342337525

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779163T>G (hg19) ; chr1:g.150806687T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806687T>G , CM000663.2:g.150806687T>G	GRCh38
NC_000001.10:g.150779163T>G , CM000663.1:g.150779163T>G	GRCh37
NC_000001.9:g.149045787T>G	NCBI36
NG_011848.1:g.6650A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.119A>C MANE Select	ENSP00000271651.3:p.Lys40Thr
ENST00000443913.2:c.296A>C	ENSP00000405083.2:p.Lys99Thr
ENST00000480670.2:n.2727A>C
ENST00000676680.1:c.119A>C	ENSP00000503270.1:p.Lys40Thr
ENST00000676716.1:c.119A>C	ENSP00000504737.1:p.Lys40Thr
ENST00000676751.1:c.119A>C	ENSP00000502964.1:p.Lys40Thr
ENST00000676824.1:c.119A>C	ENSP00000504176.1:p.Lys40Thr
ENST00000676966.1:c.119A>C	ENSP00000503723.1:p.Lys40Thr
ENST00000676970.1:c.119A>C	ENSP00000503832.1:p.Lys40Thr
ENST00000677330.1:n.1484A>C
ENST00000677887.1:c.161A>C	ENSP00000503876.1:p.Lys54Thr
ENST00000678275.1:c.119A>C	ENSP00000504796.1:p.Lys40Thr
ENST00000678337.1:c.155A>C	ENSP00000504759.1:p.Lys52Thr
ENST00000678725.1:n.1096A>C
ENST00000679090.1:n.243A>C
ENST00000679148.1:n.999A>C
ENST00000679171.1:n.2019A>C
ENST00000679260.1:c.119A>C	ENSP00000504534.1:p.Lys40Thr
ENST00000271651.7:c.119A>C	ENSP00000271651.3:p.Lys40Thr
ENST00000443913.1:c.296A>C	ENSP00000405083.1:p.Lys99Thr
ENST00000480670.1:n.82A>C
NM_000396.3:c.119A>C	NP_000387.1:p.Lys40Thr
NM_000396.4:c.119A>C MANE Select	NP_000387.1:p.Lys40Thr