Canonical Allele Identifier: CA342336752

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776693G>A (hg19) ; chr1:g.150804217G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804217G>A , CM000663.2:g.150804217G>A	GRCh38
NC_000001.10:g.150776693G>A , CM000663.1:g.150776693G>A	GRCh37
NC_000001.9:g.149043317G>A	NCBI36
NG_011848.1:g.9120C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.422C>T MANE Select	ENSP00000271651.3:p.Ala141Val
ENST00000443913.2:c.599C>T	ENSP00000405083.2:p.Ala200Val
ENST00000480670.2:n.3491C>T
ENST00000676680.1:c.422C>T	ENSP00000503270.1:p.Ala141Val
ENST00000676716.1:c.299C>T	ENSP00000504737.1:p.Ala100Val
ENST00000676751.1:c.422C>T	ENSP00000502964.1:p.Ala141Val
ENST00000676824.1:c.422C>T	ENSP00000504176.1:p.Ala141Val
ENST00000676966.1:c.422C>T	ENSP00000503723.1:p.Ala141Val
ENST00000676970.1:c.422C>T	ENSP00000503832.1:p.Ala141Val
ENST00000677330.1:n.2248C>T
ENST00000677611.1:n.274C>T
ENST00000677887.1:c.464C>T	ENSP00000503876.1:p.Ala155Val
ENST00000678275.1:c.*314C>T	ENSP00000504796.1:n.*314C>T
ENST00000678337.1:c.458C>T	ENSP00000504759.1:p.Ala153Val
ENST00000678725.1:n.1399C>T
ENST00000679090.1:n.1007C>T
ENST00000679148.1:n.3384C>T
ENST00000679171.1:n.2783C>T
ENST00000679260.1:c.399+1644C>T	ENSP00000504534.1:n.399+1644C>T
ENST00000271651.7:c.422C>T	ENSP00000271651.3:p.Ala141Val
ENST00000443913.1:c.599C>T	ENSP00000405083.1:p.Ala200Val
ENST00000480670.1:n.262C>T
NM_000396.3:c.422C>T	NP_000387.1:p.Ala141Val
NM_000396.4:c.422C>T MANE Select	NP_000387.1:p.Ala141Val