Canonical Allele Identifier: CA420699492

Gene: CTSK

Linked Data

• dbSNP Id: rs1571126416
• MyVariant Identifiers: chr1:g.150776692A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804216A>G , CM000663.2:g.150804216A>G	GRCh38
NC_000001.10:g.150776692A>G , CM000663.1:g.150776692A>G	GRCh37
NC_000001.9:g.149043316A>G	NCBI36
NG_011848.1:g.9121T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.423T>C MANE Select	ENSP00000271651.3:p.Ala141=
ENST00000443913.2:c.600T>C	ENSP00000405083.2:p.Ala200=
ENST00000480670.2:n.3492T>C
ENST00000676680.1:c.423T>C	ENSP00000503270.1:p.Ala141=
ENST00000676716.1:c.300T>C	ENSP00000504737.1:p.Ala100=
ENST00000676751.1:c.423T>C	ENSP00000502964.1:p.Ala141=
ENST00000676824.1:c.423T>C	ENSP00000504176.1:p.Ala141=
ENST00000676966.1:c.423T>C	ENSP00000503723.1:p.Ala141=
ENST00000676970.1:c.423T>C	ENSP00000503832.1:p.Ala141=
ENST00000677330.1:n.2249T>C
ENST00000677611.1:n.275T>C
ENST00000677887.1:c.465T>C	ENSP00000503876.1:p.Ala155=
ENST00000678275.1:c.*315T>C	ENSP00000504796.1:n.*315T>C
ENST00000678337.1:c.459T>C	ENSP00000504759.1:p.Ala153=
ENST00000678725.1:n.1400T>C
ENST00000679090.1:n.1008T>C
ENST00000679148.1:n.3385T>C
ENST00000679171.1:n.2784T>C
ENST00000679260.1:c.399+1645T>C	ENSP00000504534.1:n.399+1645T>C
ENST00000271651.7:c.423T>C	ENSP00000271651.3:p.Ala141=
ENST00000443913.1:c.600T>C	ENSP00000405083.1:p.Ala200=
ENST00000480670.1:n.263T>C
NM_000396.3:c.423T>C	NP_000387.1:p.Ala141=
NM_000396.4:c.423T>C MANE Select	NP_000387.1:p.Ala141=