Canonical Allele Identifier: CA342336524

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776589C>T (hg19) ; chr1:g.150804113C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804113C>T , CM000663.2:g.150804113C>T	GRCh38
NC_000001.10:g.150776589C>T , CM000663.1:g.150776589C>T	GRCh37
NC_000001.9:g.149043213C>T	NCBI36
NG_011848.1:g.9224G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.526G>A MANE Select	ENSP00000271651.3:p.Gly176Ser
ENST00000443913.2:c.703G>A	ENSP00000405083.2:p.Gly235Ser
ENST00000480670.2:n.3595G>A
ENST00000676680.1:c.526G>A	ENSP00000503270.1:p.Gly176Ser
ENST00000676716.1:c.403G>A	ENSP00000504737.1:p.Gly135Ser
ENST00000676751.1:c.526G>A	ENSP00000502964.1:p.Gly176Ser
ENST00000676824.1:c.526G>A	ENSP00000504176.1:p.Gly176Ser
ENST00000676966.1:c.526G>A	ENSP00000503723.1:p.Gly176Ser
ENST00000676970.1:c.526G>A	ENSP00000503832.1:p.Gly176Ser
ENST00000677330.1:n.2352G>A
ENST00000677611.1:n.378G>A
ENST00000677887.1:c.568G>A	ENSP00000503876.1:p.Gly190Ser
ENST00000678275.1:c.*418G>A	ENSP00000504796.1:n.*418G>A
ENST00000678337.1:c.562G>A	ENSP00000504759.1:p.Gly188Ser
ENST00000678725.1:n.1503G>A
ENST00000679090.1:n.1111G>A
ENST00000679148.1:n.3488G>A
ENST00000679171.1:n.2887G>A
ENST00000679260.1:c.399+1748G>A	ENSP00000504534.1:n.399+1748G>A
ENST00000271651.7:c.526G>A	ENSP00000271651.3:p.Gly176Ser
ENST00000443913.1:c.703G>A	ENSP00000405083.1:p.Gly235Ser
ENST00000480670.1:n.366G>A
NM_000396.3:c.526G>A	NP_000387.1:p.Gly176Ser
NM_000396.4:c.526G>A MANE Select	NP_000387.1:p.Gly176Ser