Canonical Allele Identifier: CA420701492

Gene: CTSK

Linked Data

• dbSNP Id: rs1055444697
• gnomAD v4: 1-150806770-C-T
• MyVariant Identifiers: chr1:g.150779246C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806770C>T , CM000663.2:g.150806770C>T	GRCh38
NC_000001.10:g.150779246C>T , CM000663.1:g.150779246C>T	GRCh37
NC_000001.9:g.149045870C>T	NCBI36
NG_011848.1:g.6567G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.36G>A MANE Select	ENSP00000271651.3:p.Val12=
ENST00000443913.2:c.213G>A	ENSP00000405083.2:p.Val71=
ENST00000480670.2:n.2644G>A
ENST00000676680.1:c.36G>A	ENSP00000503270.1:p.Val12=
ENST00000676716.1:c.36G>A	ENSP00000504737.1:p.Val12=
ENST00000676751.1:c.36G>A	ENSP00000502964.1:p.Val12=
ENST00000676824.1:c.36G>A	ENSP00000504176.1:p.Val12=
ENST00000676966.1:c.36G>A	ENSP00000503723.1:p.Val12=
ENST00000676970.1:c.36G>A	ENSP00000503832.1:p.Val12=
ENST00000677330.1:n.1401G>A
ENST00000677887.1:c.78G>A	ENSP00000503876.1:p.Val26=
ENST00000678275.1:c.36G>A	ENSP00000504796.1:p.Val12=
ENST00000678337.1:c.72G>A	ENSP00000504759.1:p.Val24=
ENST00000678725.1:n.1013G>A
ENST00000679090.1:n.160G>A
ENST00000679148.1:n.916G>A
ENST00000679171.1:n.1936G>A
ENST00000679260.1:c.36G>A	ENSP00000504534.1:p.Val12=
ENST00000271651.7:c.36G>A	ENSP00000271651.3:p.Val12=
ENST00000443913.1:c.213G>A	ENSP00000405083.1:p.Val71=
NM_000396.3:c.36G>A	NP_000387.1:p.Val12=
NM_000396.4:c.36G>A MANE Select	NP_000387.1:p.Val12=