Canonical Allele Identifier: CA420699356

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776500T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804024T>C , CM000663.2:g.150804024T>C	GRCh38
NC_000001.10:g.150776500T>C , CM000663.1:g.150776500T>C	GRCh37
NC_000001.9:g.149043124T>C	NCBI36
NG_011848.1:g.9313A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.615A>G MANE Select	ENSP00000271651.3:p.Gly205=
ENST00000443913.2:c.792A>G	ENSP00000405083.2:p.Gly264=
ENST00000480670.2:n.3684A>G
ENST00000676680.1:c.615A>G	ENSP00000503270.1:p.Gly205=
ENST00000676716.1:c.492A>G	ENSP00000504737.1:p.Gly164=
ENST00000676751.1:c.615A>G	ENSP00000502964.1:p.Gly205=
ENST00000676824.1:c.615A>G	ENSP00000504176.1:p.Gly205=
ENST00000676966.1:c.615A>G	ENSP00000503723.1:p.Gly205=
ENST00000676970.1:c.615A>G	ENSP00000503832.1:p.Gly205=
ENST00000677330.1:n.2441A>G
ENST00000677611.1:n.467A>G
ENST00000677887.1:c.657A>G	ENSP00000503876.1:p.Gly219=
ENST00000678275.1:c.*507A>G	ENSP00000504796.1:n.*507A>G
ENST00000678337.1:c.651A>G	ENSP00000504759.1:p.Gly217=
ENST00000678725.1:n.1592A>G
ENST00000679090.1:n.1200A>G
ENST00000679148.1:n.3577A>G
ENST00000679171.1:n.2976A>G
ENST00000679260.1:c.399+1837A>G	ENSP00000504534.1:n.399+1837A>G
ENST00000271651.7:c.615A>G	ENSP00000271651.3:p.Gly205=
ENST00000480670.1:n.455A>G
NM_000396.3:c.615A>G	NP_000387.1:p.Gly205=
NM_000396.4:c.615A>G MANE Select	NP_000387.1:p.Gly205=