Canonical Allele Identifier: CA420706373

Gene: CTSK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796862G>A , CM000663.2:g.150796862G>A	GRCh38
NC_000001.10:g.150769338G>A , CM000663.1:g.150769338G>A	GRCh37
NC_000001.9:g.149035962G>A	NCBI36
NG_011848.1:g.16475C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.927C>T MANE Select	ENSP00000271651.3:p.Leu309=
ENST00000443913.2:c.1104C>T	ENSP00000405083.2:p.Leu368=
ENST00000480670.2:n.3996C>T
ENST00000676680.1:c.*221C>T	ENSP00000503270.1:n.*221C>T
ENST00000676716.1:c.804C>T	ENSP00000504737.1:p.Leu268=
ENST00000676751.1:c.821C>T	ENSP00000502964.1:p.Ser274Leu
ENST00000676824.1:c.927C>T	ENSP00000504176.1:p.Leu309=
ENST00000676966.1:c.927C>T	ENSP00000503723.1:p.Leu309=
ENST00000676970.1:c.939C>T	ENSP00000503832.1:p.Leu313=
ENST00000677330.1:n.2753C>T
ENST00000677611.1:n.779C>T
ENST00000677887.1:c.969C>T	ENSP00000503876.1:p.Leu323=
ENST00000678275.1:c.*819C>T	ENSP00000504796.1:n.*819C>T
ENST00000678337.1:c.963C>T	ENSP00000504759.1:p.Leu321=
ENST00000678725.1:n.2174C>T
ENST00000679090.1:n.1782C>T
ENST00000679148.1:n.3889C>T
ENST00000679171.1:n.3558C>T
ENST00000679178.1:n.638C>T
ENST00000679260.1:c.708C>T	ENSP00000504534.1:p.Leu236=
ENST00000271651.7:c.927C>T	ENSP00000271651.3:p.Leu309=
NM_000396.3:c.927C>T	NP_000387.1:p.Leu309=
NM_000396.4:c.927C>T MANE Select	NP_000387.1:p.Leu309=