Canonical Allele Identifier: CA342337718

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779247A>C (hg19) ; chr1:g.150806771A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806771A>C , CM000663.2:g.150806771A>C	GRCh38
NC_000001.10:g.150779247A>C , CM000663.1:g.150779247A>C	GRCh37
NC_000001.9:g.149045871A>C	NCBI36
NG_011848.1:g.6566T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.35T>G MANE Select	ENSP00000271651.3:p.Val12Gly
ENST00000443913.2:c.212T>G	ENSP00000405083.2:p.Val71Gly
ENST00000480670.2:n.2643T>G
ENST00000676680.1:c.35T>G	ENSP00000503270.1:p.Val12Gly
ENST00000676716.1:c.35T>G	ENSP00000504737.1:p.Val12Gly
ENST00000676751.1:c.35T>G	ENSP00000502964.1:p.Val12Gly
ENST00000676824.1:c.35T>G	ENSP00000504176.1:p.Val12Gly
ENST00000676966.1:c.35T>G	ENSP00000503723.1:p.Val12Gly
ENST00000676970.1:c.35T>G	ENSP00000503832.1:p.Val12Gly
ENST00000677330.1:n.1400T>G
ENST00000677887.1:c.77T>G	ENSP00000503876.1:p.Val26Gly
ENST00000678275.1:c.35T>G	ENSP00000504796.1:p.Val12Gly
ENST00000678337.1:c.71T>G	ENSP00000504759.1:p.Val24Gly
ENST00000678725.1:n.1012T>G
ENST00000679090.1:n.159T>G
ENST00000679148.1:n.915T>G
ENST00000679171.1:n.1935T>G
ENST00000679260.1:c.35T>G	ENSP00000504534.1:p.Val12Gly
ENST00000271651.7:c.35T>G	ENSP00000271651.3:p.Val12Gly
ENST00000443913.1:c.212T>G	ENSP00000405083.1:p.Val71Gly
NM_000396.3:c.35T>G	NP_000387.1:p.Val12Gly
NM_000396.4:c.35T>G MANE Select	NP_000387.1:p.Val12Gly