Canonical Allele Identifier: CA30097771

Gene: CTSK

Linked Data

• dbSNP Id: rs200143154
• gnomAD v4: 1-150804144-C-T
• COSMIC: COSM5777917 ; COSM5777918
• MyVariant Identifiers: chr1:g.150776620C>T (hg19) ; chr1:g.150804144C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804144C>T , CM000663.2:g.150804144C>T	GRCh38
NC_000001.10:g.150776620C>T , CM000663.1:g.150776620C>T	GRCh37
NC_000001.9:g.149043244C>T	NCBI36
NG_011848.1:g.9193G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.495G>A MANE Select	ENSP00000271651.3:p.Gln165=
ENST00000443913.2:c.672G>A	ENSP00000405083.2:p.Gln224=
ENST00000480670.2:n.3564G>A
ENST00000676680.1:c.495G>A	ENSP00000503270.1:p.Gln165=
ENST00000676716.1:c.372G>A	ENSP00000504737.1:p.Gln124=
ENST00000676751.1:c.495G>A	ENSP00000502964.1:p.Gln165=
ENST00000676824.1:c.495G>A	ENSP00000504176.1:p.Gln165=
ENST00000676966.1:c.495G>A	ENSP00000503723.1:p.Gln165=
ENST00000676970.1:c.495G>A	ENSP00000503832.1:p.Gln165=
ENST00000677330.1:n.2321G>A
ENST00000677611.1:n.347G>A
ENST00000677887.1:c.537G>A	ENSP00000503876.1:p.Gln179=
ENST00000678275.1:c.*387G>A	ENSP00000504796.1:n.*387G>A
ENST00000678337.1:c.531G>A	ENSP00000504759.1:p.Gln177=
ENST00000678725.1:n.1472G>A
ENST00000679090.1:n.1080G>A
ENST00000679148.1:n.3457G>A
ENST00000679171.1:n.2856G>A
ENST00000679260.1:c.399+1717G>A	ENSP00000504534.1:n.399+1717G>A
ENST00000271651.7:c.495G>A	ENSP00000271651.3:p.Gln165=
ENST00000443913.1:c.672G>A	ENSP00000405083.1:p.Gln224=
ENST00000480670.1:n.335G>A
NM_000396.3:c.495G>A	NP_000387.1:p.Gln165=
NM_000396.4:c.495G>A MANE Select	NP_000387.1:p.Gln165=