Canonical Allele Identifier: CA420699460

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776647A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804171A>G , CM000663.2:g.150804171A>G	GRCh38
NC_000001.10:g.150776647A>G , CM000663.1:g.150776647A>G	GRCh37
NC_000001.9:g.149043271A>G	NCBI36
NG_011848.1:g.9166T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.468T>C MANE Select	ENSP00000271651.3:p.Thr156=
ENST00000443913.2:c.645T>C	ENSP00000405083.2:p.Thr215=
ENST00000480670.2:n.3537T>C
ENST00000676680.1:c.468T>C	ENSP00000503270.1:p.Thr156=
ENST00000676716.1:c.345T>C	ENSP00000504737.1:p.Thr115=
ENST00000676751.1:c.468T>C	ENSP00000502964.1:p.Thr156=
ENST00000676824.1:c.468T>C	ENSP00000504176.1:p.Thr156=
ENST00000676966.1:c.468T>C	ENSP00000503723.1:p.Thr156=
ENST00000676970.1:c.468T>C	ENSP00000503832.1:p.Thr156=
ENST00000677330.1:n.2294T>C
ENST00000677611.1:n.320T>C
ENST00000677887.1:c.510T>C	ENSP00000503876.1:p.Thr170=
ENST00000678275.1:c.*360T>C	ENSP00000504796.1:n.*360T>C
ENST00000678337.1:c.504T>C	ENSP00000504759.1:p.Thr168=
ENST00000678725.1:n.1445T>C
ENST00000679090.1:n.1053T>C
ENST00000679148.1:n.3430T>C
ENST00000679171.1:n.2829T>C
ENST00000679260.1:c.399+1690T>C	ENSP00000504534.1:n.399+1690T>C
ENST00000271651.7:c.468T>C	ENSP00000271651.3:p.Thr156=
ENST00000443913.1:c.645T>C	ENSP00000405083.1:p.Thr215=
ENST00000480670.1:n.308T>C
NM_000396.3:c.468T>C	NP_000387.1:p.Thr156=
NM_000396.4:c.468T>C MANE Select	NP_000387.1:p.Thr156=