Canonical Allele Identifier: CA420699424

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776587G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804111G>T , CM000663.2:g.150804111G>T	GRCh38
NC_000001.10:g.150776587G>T , CM000663.1:g.150776587G>T	GRCh37
NC_000001.9:g.149043211G>T	NCBI36
NG_011848.1:g.9226C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.528C>A MANE Select	ENSP00000271651.3:p.Gly176=
ENST00000443913.2:c.705C>A	ENSP00000405083.2:p.Gly235=
ENST00000480670.2:n.3597C>A
ENST00000676680.1:c.528C>A	ENSP00000503270.1:p.Gly176=
ENST00000676716.1:c.405C>A	ENSP00000504737.1:p.Gly135=
ENST00000676751.1:c.528C>A	ENSP00000502964.1:p.Gly176=
ENST00000676824.1:c.528C>A	ENSP00000504176.1:p.Gly176=
ENST00000676966.1:c.528C>A	ENSP00000503723.1:p.Gly176=
ENST00000676970.1:c.528C>A	ENSP00000503832.1:p.Gly176=
ENST00000677330.1:n.2354C>A
ENST00000677611.1:n.380C>A
ENST00000677887.1:c.570C>A	ENSP00000503876.1:p.Gly190=
ENST00000678275.1:c.*420C>A	ENSP00000504796.1:n.*420C>A
ENST00000678337.1:c.564C>A	ENSP00000504759.1:p.Gly188=
ENST00000678725.1:n.1505C>A
ENST00000679090.1:n.1113C>A
ENST00000679148.1:n.3490C>A
ENST00000679171.1:n.2889C>A
ENST00000679260.1:c.399+1750C>A	ENSP00000504534.1:n.399+1750C>A
ENST00000271651.7:c.528C>A	ENSP00000271651.3:p.Gly176=
ENST00000443913.1:c.705C>A	ENSP00000405083.1:p.Gly235=
ENST00000480670.1:n.368C>A
NM_000396.3:c.528C>A	NP_000387.1:p.Gly176=
NM_000396.4:c.528C>A MANE Select	NP_000387.1:p.Gly176=