Canonical Allele Identifier: CA342337699

Gene: CTSK

Linked Data

• gnomAD v4: 1-150806762-G-A
• MyVariant Identifiers: chr1:g.150779238G>A (hg19) ; chr1:g.150806762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806762G>A , CM000663.2:g.150806762G>A	GRCh38
NC_000001.10:g.150779238G>A , CM000663.1:g.150779238G>A	GRCh37
NC_000001.9:g.149045862G>A	NCBI36
NG_011848.1:g.6575C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.44C>T MANE Select	ENSP00000271651.3:p.Ala15Val
ENST00000443913.2:c.221C>T	ENSP00000405083.2:p.Ala74Val
ENST00000480670.2:n.2652C>T
ENST00000676680.1:c.44C>T	ENSP00000503270.1:p.Ala15Val
ENST00000676716.1:c.44C>T	ENSP00000504737.1:p.Ala15Val
ENST00000676751.1:c.44C>T	ENSP00000502964.1:p.Ala15Val
ENST00000676824.1:c.44C>T	ENSP00000504176.1:p.Ala15Val
ENST00000676966.1:c.44C>T	ENSP00000503723.1:p.Ala15Val
ENST00000676970.1:c.44C>T	ENSP00000503832.1:p.Ala15Val
ENST00000677330.1:n.1409C>T
ENST00000677887.1:c.86C>T	ENSP00000503876.1:p.Ala29Val
ENST00000678275.1:c.44C>T	ENSP00000504796.1:p.Ala15Val
ENST00000678337.1:c.80C>T	ENSP00000504759.1:p.Ala27Val
ENST00000678725.1:n.1021C>T
ENST00000679090.1:n.168C>T
ENST00000679148.1:n.924C>T
ENST00000679171.1:n.1944C>T
ENST00000679260.1:c.44C>T	ENSP00000504534.1:p.Ala15Val
ENST00000271651.7:c.44C>T	ENSP00000271651.3:p.Ala15Val
ENST00000443913.1:c.221C>T	ENSP00000405083.1:p.Ala74Val
ENST00000480670.1:n.7C>T
NM_000396.3:c.44C>T	NP_000387.1:p.Ala15Val
NM_000396.4:c.44C>T MANE Select	NP_000387.1:p.Ala15Val