Canonical Allele Identifier: CA420699371

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776515G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804039G>T , CM000663.2:g.150804039G>T	GRCh38
NC_000001.10:g.150776515G>T , CM000663.1:g.150776515G>T	GRCh37
NC_000001.9:g.149043139G>T	NCBI36
NG_011848.1:g.9298C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.600C>A MANE Select	ENSP00000271651.3:p.Ala200=
ENST00000443913.2:c.777C>A	ENSP00000405083.2:p.Ala259=
ENST00000480670.2:n.3669C>A
ENST00000676680.1:c.600C>A	ENSP00000503270.1:p.Ala200=
ENST00000676716.1:c.477C>A	ENSP00000504737.1:p.Ala159=
ENST00000676751.1:c.600C>A	ENSP00000502964.1:p.Ala200=
ENST00000676824.1:c.600C>A	ENSP00000504176.1:p.Ala200=
ENST00000676966.1:c.600C>A	ENSP00000503723.1:p.Ala200=
ENST00000676970.1:c.600C>A	ENSP00000503832.1:p.Ala200=
ENST00000677330.1:n.2426C>A
ENST00000677611.1:n.452C>A
ENST00000677887.1:c.642C>A	ENSP00000503876.1:p.Ala214=
ENST00000678275.1:c.*492C>A	ENSP00000504796.1:n.*492C>A
ENST00000678337.1:c.636C>A	ENSP00000504759.1:p.Ala212=
ENST00000678725.1:n.1577C>A
ENST00000679090.1:n.1185C>A
ENST00000679148.1:n.3562C>A
ENST00000679171.1:n.2961C>A
ENST00000679260.1:c.399+1822C>A	ENSP00000504534.1:n.399+1822C>A
ENST00000271651.7:c.600C>A	ENSP00000271651.3:p.Ala200=
ENST00000480670.1:n.440C>A
NM_000396.3:c.600C>A	NP_000387.1:p.Ala200=
NM_000396.4:c.600C>A MANE Select	NP_000387.1:p.Ala200=