Canonical Allele Identifier: CA526062925

Gene: CTSK

Linked Data

• dbSNP Id: rs1251563081
• gnomAD v2: 1-150779139-G-GC
• MyVariant Identifiers: chr1:g.150779139_150779140insC (hg19) ; chr1:g.150806663_150806664insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806668dup , CM000663.2:g.150806668dup	GRCh38
NC_000001.10:g.150779144dup , CM000663.1:g.150779144dup	GRCh37
NC_000001.9:g.149045768dup	NCBI36
NG_011848.1:g.6673dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.120+22dup MANE Select	ENSP00000271651.3:n.120+22dup
ENST00000443913.2:c.297+22dup	ENSP00000405083.2:n.297+22dup
ENST00000480670.2:n.2750dup
ENST00000676680.1:c.120+22dup	ENSP00000503270.1:n.120+22dup
ENST00000676716.1:c.120+22dup	ENSP00000504737.1:n.120+22dup
ENST00000676751.1:c.120+22dup	ENSP00000502964.1:n.120+22dup
ENST00000676824.1:c.120+22dup	ENSP00000504176.1:n.120+22dup
ENST00000676966.1:c.120+22dup	ENSP00000503723.1:n.120+22dup
ENST00000676970.1:c.120+22dup	ENSP00000503832.1:n.120+22dup
ENST00000677330.1:n.1507dup
ENST00000677887.1:c.162+22dup	ENSP00000503876.1:n.162+22dup
ENST00000678275.1:c.120+22dup	ENSP00000504796.1:n.120+22dup
ENST00000678337.1:c.156+22dup	ENSP00000504759.1:n.156+22dup
ENST00000678725.1:n.1097+22dup
ENST00000679090.1:n.266dup
ENST00000679148.1:n.1022dup
ENST00000679171.1:n.2042dup
ENST00000679260.1:c.120+22dup	ENSP00000504534.1:n.120+22dup
ENST00000271651.7:c.120+22dup	ENSP00000271651.3:n.120+22dup
ENST00000443913.1:c.297+22dup	ENSP00000405083.1:n.297+22dup
ENST00000480670.1:n.83+22dup
NM_000396.3:c.120+22dup	NP_000387.1:n.120+22dup
NM_000396.4:c.120+22dup MANE Select	NP_000387.1:n.120+22dup