Canonical Allele Identifier: CA420699486

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776683A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804207A>C , CM000663.2:g.150804207A>C	GRCh38
NC_000001.10:g.150776683A>C , CM000663.1:g.150776683A>C	GRCh37
NC_000001.9:g.149043307A>C	NCBI36
NG_011848.1:g.9130T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.432T>G MANE Select	ENSP00000271651.3:p.Ser144=
ENST00000443913.2:c.609T>G	ENSP00000405083.2:p.Ser203=
ENST00000480670.2:n.3501T>G
ENST00000676680.1:c.432T>G	ENSP00000503270.1:p.Ser144=
ENST00000676716.1:c.309T>G	ENSP00000504737.1:p.Ser103=
ENST00000676751.1:c.432T>G	ENSP00000502964.1:p.Ser144=
ENST00000676824.1:c.432T>G	ENSP00000504176.1:p.Ser144=
ENST00000676966.1:c.432T>G	ENSP00000503723.1:p.Ser144=
ENST00000676970.1:c.432T>G	ENSP00000503832.1:p.Ser144=
ENST00000677330.1:n.2258T>G
ENST00000677611.1:n.284T>G
ENST00000677887.1:c.474T>G	ENSP00000503876.1:p.Ser158=
ENST00000678275.1:c.*324T>G	ENSP00000504796.1:n.*324T>G
ENST00000678337.1:c.468T>G	ENSP00000504759.1:p.Ser156=
ENST00000678725.1:n.1409T>G
ENST00000679090.1:n.1017T>G
ENST00000679148.1:n.3394T>G
ENST00000679171.1:n.2793T>G
ENST00000679260.1:c.399+1654T>G	ENSP00000504534.1:n.399+1654T>G
ENST00000271651.7:c.432T>G	ENSP00000271651.3:p.Ser144=
ENST00000443913.1:c.609T>G	ENSP00000405083.1:p.Ser203=
ENST00000480670.1:n.272T>G
NM_000396.3:c.432T>G	NP_000387.1:p.Ser144=
NM_000396.4:c.432T>G MANE Select	NP_000387.1:p.Ser144=