Canonical Allele Identifier: CA342335631

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796882C>T , CM000663.2:g.150796882C>T	GRCh38
NC_000001.10:g.150769358C>T , CM000663.1:g.150769358C>T	GRCh37
NC_000001.9:g.149035982C>T	NCBI36
NG_011848.1:g.16455G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.907G>A MANE Select	NP_000387.1:p.Gly303Arg
ENST00000271651.8:c.907G>A MANE Select	ENSP00000271651.3:p.Gly303Arg
NM_000396.3:c.907G>A	NP_000387.1:p.Gly303Arg
ENST00000271651.7:c.907G>A	ENSP00000271651.3:p.Gly303Arg
ENST00000443913.2:c.1084G>A	ENSP00000405083.2:p.Gly362Arg
ENST00000480670.2:n.3976G>A
ENST00000676680.1:c.*201G>A	ENSP00000503270.1:n.*201G>A
ENST00000676716.1:c.784G>A	ENSP00000504737.1:p.Gly262Arg
ENST00000676751.1:c.801G>A	ENSP00000502964.1:p.Gly267=
ENST00000676824.1:c.907G>A	ENSP00000504176.1:p.Gly303Arg
ENST00000676966.1:c.907G>A	ENSP00000503723.1:p.Gly303Arg
ENST00000676970.1:c.919G>A	ENSP00000503832.1:p.Gly307Arg
ENST00000677330.1:n.2733G>A
ENST00000677611.1:n.759G>A
ENST00000677887.1:c.949G>A	ENSP00000503876.1:p.Gly317Arg
ENST00000678275.1:c.*799G>A	ENSP00000504796.1:n.*799G>A
ENST00000678337.1:c.943G>A	ENSP00000504759.1:p.Gly315Arg
ENST00000678725.1:n.2154G>A
ENST00000679090.1:n.1762G>A
ENST00000679148.1:n.3869G>A
ENST00000679171.1:n.3538G>A
ENST00000679178.1:n.618G>A
ENST00000679260.1:c.688G>A	ENSP00000504534.1:p.Gly230Arg