Canonical Allele Identifier: CA342336694

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776666C>A (hg19) ; chr1:g.150804190C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804190C>A , CM000663.2:g.150804190C>A	GRCh38
NC_000001.10:g.150776666C>A , CM000663.1:g.150776666C>A	GRCh37
NC_000001.9:g.149043290C>A	NCBI36
NG_011848.1:g.9147G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.449G>T MANE Select	ENSP00000271651.3:p.Gly150Val
ENST00000443913.2:c.626G>T	ENSP00000405083.2:p.Gly209Val
ENST00000480670.2:n.3518G>T
ENST00000676680.1:c.449G>T	ENSP00000503270.1:p.Gly150Val
ENST00000676716.1:c.326G>T	ENSP00000504737.1:p.Gly109Val
ENST00000676751.1:c.449G>T	ENSP00000502964.1:p.Gly150Val
ENST00000676824.1:c.449G>T	ENSP00000504176.1:p.Gly150Val
ENST00000676966.1:c.449G>T	ENSP00000503723.1:p.Gly150Val
ENST00000676970.1:c.449G>T	ENSP00000503832.1:p.Gly150Val
ENST00000677330.1:n.2275G>T
ENST00000677611.1:n.301G>T
ENST00000677887.1:c.491G>T	ENSP00000503876.1:p.Gly164Val
ENST00000678275.1:c.*341G>T	ENSP00000504796.1:n.*341G>T
ENST00000678337.1:c.485G>T	ENSP00000504759.1:p.Gly162Val
ENST00000678725.1:n.1426G>T
ENST00000679090.1:n.1034G>T
ENST00000679148.1:n.3411G>T
ENST00000679171.1:n.2810G>T
ENST00000679260.1:c.399+1671G>T	ENSP00000504534.1:n.399+1671G>T
ENST00000271651.7:c.449G>T	ENSP00000271651.3:p.Gly150Val
ENST00000443913.1:c.626G>T	ENSP00000405083.1:p.Gly209Val
ENST00000480670.1:n.289G>T
NM_000396.3:c.449G>T	NP_000387.1:p.Gly150Val
NM_000396.4:c.449G>T MANE Select	NP_000387.1:p.Gly150Val