Canonical Allele Identifier: CA420699407

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776560G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804084G>C , CM000663.2:g.150804084G>C	GRCh38
NC_000001.10:g.150776560G>C , CM000663.1:g.150776560G>C	GRCh37
NC_000001.9:g.149043184G>C	NCBI36
NG_011848.1:g.9253C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.555C>G MANE Select	ENSP00000271651.3:p.Ala185=
ENST00000443913.2:c.732C>G	ENSP00000405083.2:p.Ala244=
ENST00000480670.2:n.3624C>G
ENST00000676680.1:c.555C>G	ENSP00000503270.1:p.Ala185=
ENST00000676716.1:c.432C>G	ENSP00000504737.1:p.Ala144=
ENST00000676751.1:c.555C>G	ENSP00000502964.1:p.Ala185=
ENST00000676824.1:c.555C>G	ENSP00000504176.1:p.Ala185=
ENST00000676966.1:c.555C>G	ENSP00000503723.1:p.Ala185=
ENST00000676970.1:c.555C>G	ENSP00000503832.1:p.Ala185=
ENST00000677330.1:n.2381C>G
ENST00000677611.1:n.407C>G
ENST00000677887.1:c.597C>G	ENSP00000503876.1:p.Ala199=
ENST00000678275.1:c.*447C>G	ENSP00000504796.1:n.*447C>G
ENST00000678337.1:c.591C>G	ENSP00000504759.1:p.Ala197=
ENST00000678725.1:n.1532C>G
ENST00000679090.1:n.1140C>G
ENST00000679148.1:n.3517C>G
ENST00000679171.1:n.2916C>G
ENST00000679260.1:c.399+1777C>G	ENSP00000504534.1:n.399+1777C>G
ENST00000271651.7:c.555C>G	ENSP00000271651.3:p.Ala185=
ENST00000443913.1:c.732C>G	ENSP00000405083.1:p.Ala244=
ENST00000480670.1:n.395C>G
NM_000396.3:c.555C>G	NP_000387.1:p.Ala185=
NM_000396.4:c.555C>G MANE Select	NP_000387.1:p.Ala185=