Canonical Allele Identifier: CA420699402

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776548C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804072C>G , CM000663.2:g.150804072C>G	GRCh38
NC_000001.10:g.150776548C>G , CM000663.1:g.150776548C>G	GRCh37
NC_000001.9:g.149043172C>G	NCBI36
NG_011848.1:g.9265G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.567G>C MANE Select	ENSP00000271651.3:p.Val189=
ENST00000443913.2:c.744G>C	ENSP00000405083.2:p.Val248=
ENST00000480670.2:n.3636G>C
ENST00000676680.1:c.567G>C	ENSP00000503270.1:p.Val189=
ENST00000676716.1:c.444G>C	ENSP00000504737.1:p.Val148=
ENST00000676751.1:c.567G>C	ENSP00000502964.1:p.Val189=
ENST00000676824.1:c.567G>C	ENSP00000504176.1:p.Val189=
ENST00000676966.1:c.567G>C	ENSP00000503723.1:p.Val189=
ENST00000676970.1:c.567G>C	ENSP00000503832.1:p.Val189=
ENST00000677330.1:n.2393G>C
ENST00000677611.1:n.419G>C
ENST00000677887.1:c.609G>C	ENSP00000503876.1:p.Val203=
ENST00000678275.1:c.*459G>C	ENSP00000504796.1:n.*459G>C
ENST00000678337.1:c.603G>C	ENSP00000504759.1:p.Val201=
ENST00000678725.1:n.1544G>C
ENST00000679090.1:n.1152G>C
ENST00000679148.1:n.3529G>C
ENST00000679171.1:n.2928G>C
ENST00000679260.1:c.399+1789G>C	ENSP00000504534.1:n.399+1789G>C
ENST00000271651.7:c.567G>C	ENSP00000271651.3:p.Val189=
ENST00000443913.1:c.744G>C	ENSP00000405083.1:p.Val248=
ENST00000480670.1:n.407G>C
NM_000396.3:c.567G>C	NP_000387.1:p.Val189=
NM_000396.4:c.567G>C MANE Select	NP_000387.1:p.Val189=