Canonical Allele Identifier: CA420699423

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804108-A-G
• MyVariant Identifiers: chr1:g.150776584A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804108A>G , CM000663.2:g.150804108A>G	GRCh38
NC_000001.10:g.150776584A>G , CM000663.1:g.150776584A>G	GRCh37
NC_000001.9:g.149043208A>G	NCBI36
NG_011848.1:g.9229T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.531T>C MANE Select	ENSP00000271651.3:p.Cys177=
ENST00000443913.2:c.708T>C	ENSP00000405083.2:p.Cys236=
ENST00000480670.2:n.3600T>C
ENST00000676680.1:c.531T>C	ENSP00000503270.1:p.Cys177=
ENST00000676716.1:c.408T>C	ENSP00000504737.1:p.Cys136=
ENST00000676751.1:c.531T>C	ENSP00000502964.1:p.Cys177=
ENST00000676824.1:c.531T>C	ENSP00000504176.1:p.Cys177=
ENST00000676966.1:c.531T>C	ENSP00000503723.1:p.Cys177=
ENST00000676970.1:c.531T>C	ENSP00000503832.1:p.Cys177=
ENST00000677330.1:n.2357T>C
ENST00000677611.1:n.383T>C
ENST00000677887.1:c.573T>C	ENSP00000503876.1:p.Cys191=
ENST00000678275.1:c.*423T>C	ENSP00000504796.1:n.*423T>C
ENST00000678337.1:c.567T>C	ENSP00000504759.1:p.Cys189=
ENST00000678725.1:n.1508T>C
ENST00000679090.1:n.1116T>C
ENST00000679148.1:n.3493T>C
ENST00000679171.1:n.2892T>C
ENST00000679260.1:c.399+1753T>C	ENSP00000504534.1:n.399+1753T>C
ENST00000271651.7:c.531T>C	ENSP00000271651.3:p.Cys177=
ENST00000443913.1:c.708T>C	ENSP00000405083.1:p.Cys236=
ENST00000480670.1:n.371T>C
NM_000396.3:c.531T>C	NP_000387.1:p.Cys177=
NM_000396.4:c.531T>C MANE Select	NP_000387.1:p.Cys177=