Canonical Allele Identifier: CA342337698

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779238G>T (hg19) ; chr1:g.150806762G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.44C>A MANE Select	ENSP00000271651.3:p.Ala15Asp
ENST00000443913.2:c.221C>A	ENSP00000405083.2:p.Ala74Asp
ENST00000480670.2:n.2652C>A
ENST00000676680.1:c.44C>A	ENSP00000503270.1:p.Ala15Asp
ENST00000676716.1:c.44C>A	ENSP00000504737.1:p.Ala15Asp
ENST00000676751.1:c.44C>A	ENSP00000502964.1:p.Ala15Asp
ENST00000676824.1:c.44C>A	ENSP00000504176.1:p.Ala15Asp
ENST00000676966.1:c.44C>A	ENSP00000503723.1:p.Ala15Asp
ENST00000676970.1:c.44C>A	ENSP00000503832.1:p.Ala15Asp
ENST00000677330.1:n.1409C>A
ENST00000677887.1:c.86C>A	ENSP00000503876.1:p.Ala29Asp
ENST00000678275.1:c.44C>A	ENSP00000504796.1:p.Ala15Asp
ENST00000678337.1:c.80C>A	ENSP00000504759.1:p.Ala27Asp
ENST00000678725.1:n.1021C>A
ENST00000679090.1:n.168C>A
ENST00000679148.1:n.924C>A
ENST00000679171.1:n.1944C>A
ENST00000679260.1:c.44C>A	ENSP00000504534.1:p.Ala15Asp
ENST00000271651.7:c.44C>A	ENSP00000271651.3:p.Ala15Asp
ENST00000443913.1:c.221C>A	ENSP00000405083.1:p.Ala74Asp
ENST00000480670.1:n.7C>A
NM_000396.3:c.44C>A	NP_000387.1:p.Ala15Asp
NM_000396.4:c.44C>A MANE Select	NP_000387.1:p.Ala15Asp