Canonical Allele Identifier: CA420699481

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776677A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804201A>T , CM000663.2:g.150804201A>T	GRCh38
NC_000001.10:g.150776677A>T , CM000663.1:g.150776677A>T	GRCh37
NC_000001.9:g.149043301A>T	NCBI36
NG_011848.1:g.9136T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.438T>A MANE Select	ENSP00000271651.3:p.Gly146=
ENST00000443913.2:c.615T>A	ENSP00000405083.2:p.Gly205=
ENST00000480670.2:n.3507T>A
ENST00000676680.1:c.438T>A	ENSP00000503270.1:p.Gly146=
ENST00000676716.1:c.315T>A	ENSP00000504737.1:p.Gly105=
ENST00000676751.1:c.438T>A	ENSP00000502964.1:p.Gly146=
ENST00000676824.1:c.438T>A	ENSP00000504176.1:p.Gly146=
ENST00000676966.1:c.438T>A	ENSP00000503723.1:p.Gly146=
ENST00000676970.1:c.438T>A	ENSP00000503832.1:p.Gly146=
ENST00000677330.1:n.2264T>A
ENST00000677611.1:n.290T>A
ENST00000677887.1:c.480T>A	ENSP00000503876.1:p.Gly160=
ENST00000678275.1:c.*330T>A	ENSP00000504796.1:n.*330T>A
ENST00000678337.1:c.474T>A	ENSP00000504759.1:p.Gly158=
ENST00000678725.1:n.1415T>A
ENST00000679090.1:n.1023T>A
ENST00000679148.1:n.3400T>A
ENST00000679171.1:n.2799T>A
ENST00000679260.1:c.399+1660T>A	ENSP00000504534.1:n.399+1660T>A
ENST00000271651.7:c.438T>A	ENSP00000271651.3:p.Gly146=
ENST00000443913.1:c.615T>A	ENSP00000405083.1:p.Gly205=
ENST00000480670.1:n.278T>A
NM_000396.3:c.438T>A	NP_000387.1:p.Gly146=
NM_000396.4:c.438T>A MANE Select	NP_000387.1:p.Gly146=