Canonical Allele Identifier: CA342337729

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779251C>T (hg19) ; chr1:g.150806775C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806775C>T , CM000663.2:g.150806775C>T	GRCh38
NC_000001.10:g.150779251C>T , CM000663.1:g.150779251C>T	GRCh37
NC_000001.9:g.149045875C>T	NCBI36
NG_011848.1:g.6562G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.31G>A MANE Select	ENSP00000271651.3:p.Val11Met
ENST00000443913.2:c.208G>A	ENSP00000405083.2:p.Val70Met
ENST00000480670.2:n.2639G>A
ENST00000676680.1:c.31G>A	ENSP00000503270.1:p.Val11Met
ENST00000676716.1:c.31G>A	ENSP00000504737.1:p.Val11Met
ENST00000676751.1:c.31G>A	ENSP00000502964.1:p.Val11Met
ENST00000676824.1:c.31G>A	ENSP00000504176.1:p.Val11Met
ENST00000676966.1:c.31G>A	ENSP00000503723.1:p.Val11Met
ENST00000676970.1:c.31G>A	ENSP00000503832.1:p.Val11Met
ENST00000677330.1:n.1396G>A
ENST00000677887.1:c.73G>A	ENSP00000503876.1:p.Val25Met
ENST00000678275.1:c.31G>A	ENSP00000504796.1:p.Val11Met
ENST00000678337.1:c.67G>A	ENSP00000504759.1:p.Val23Met
ENST00000678725.1:n.1008G>A
ENST00000679090.1:n.155G>A
ENST00000679148.1:n.911G>A
ENST00000679171.1:n.1931G>A
ENST00000679260.1:c.31G>A	ENSP00000504534.1:p.Val11Met
ENST00000271651.7:c.31G>A	ENSP00000271651.3:p.Val11Met
ENST00000443913.1:c.208G>A	ENSP00000405083.1:p.Val70Met
NM_000396.3:c.31G>A	NP_000387.1:p.Val11Met
NM_000396.4:c.31G>A MANE Select	NP_000387.1:p.Val11Met