Canonical Allele Identifier: CA420699420

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776581T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804105T>A , CM000663.2:g.150804105T>A	GRCh38
NC_000001.10:g.150776581T>A , CM000663.1:g.150776581T>A	GRCh37
NC_000001.9:g.149043205T>A	NCBI36
NG_011848.1:g.9232A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.534A>T MANE Select	ENSP00000271651.3:p.Gly178=
ENST00000443913.2:c.711A>T	ENSP00000405083.2:p.Gly237=
ENST00000480670.2:n.3603A>T
ENST00000676680.1:c.534A>T	ENSP00000503270.1:p.Gly178=
ENST00000676716.1:c.411A>T	ENSP00000504737.1:p.Gly137=
ENST00000676751.1:c.534A>T	ENSP00000502964.1:p.Gly178=
ENST00000676824.1:c.534A>T	ENSP00000504176.1:p.Gly178=
ENST00000676966.1:c.534A>T	ENSP00000503723.1:p.Gly178=
ENST00000676970.1:c.534A>T	ENSP00000503832.1:p.Gly178=
ENST00000677330.1:n.2360A>T
ENST00000677611.1:n.386A>T
ENST00000677887.1:c.576A>T	ENSP00000503876.1:p.Gly192=
ENST00000678275.1:c.*426A>T	ENSP00000504796.1:n.*426A>T
ENST00000678337.1:c.570A>T	ENSP00000504759.1:p.Gly190=
ENST00000678725.1:n.1511A>T
ENST00000679090.1:n.1119A>T
ENST00000679148.1:n.3496A>T
ENST00000679171.1:n.2895A>T
ENST00000679260.1:c.399+1756A>T	ENSP00000504534.1:n.399+1756A>T
ENST00000271651.7:c.534A>T	ENSP00000271651.3:p.Gly178=
ENST00000443913.1:c.711A>T	ENSP00000405083.1:p.Gly237=
ENST00000480670.1:n.374A>T
NM_000396.3:c.534A>T	NP_000387.1:p.Gly178=
NM_000396.4:c.534A>T MANE Select	NP_000387.1:p.Gly178=