Canonical Allele Identifier: CA342336367

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776518A>C (hg19) ; chr1:g.150804042A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804042A>C , CM000663.2:g.150804042A>C	GRCh38
NC_000001.10:g.150776518A>C , CM000663.1:g.150776518A>C	GRCh37
NC_000001.9:g.149043142A>C	NCBI36
NG_011848.1:g.9295T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.597T>G MANE Select	ENSP00000271651.3:p.Asp199Glu
ENST00000443913.2:c.774T>G	ENSP00000405083.2:p.Asp258Glu
ENST00000480670.2:n.3666T>G
ENST00000676680.1:c.597T>G	ENSP00000503270.1:p.Asp199Glu
ENST00000676716.1:c.474T>G	ENSP00000504737.1:p.Asp158Glu
ENST00000676751.1:c.597T>G	ENSP00000502964.1:p.Asp199Glu
ENST00000676824.1:c.597T>G	ENSP00000504176.1:p.Asp199Glu
ENST00000676966.1:c.597T>G	ENSP00000503723.1:p.Asp199Glu
ENST00000676970.1:c.597T>G	ENSP00000503832.1:p.Asp199Glu
ENST00000677330.1:n.2423T>G
ENST00000677611.1:n.449T>G
ENST00000677887.1:c.639T>G	ENSP00000503876.1:p.Asp213Glu
ENST00000678275.1:c.*489T>G	ENSP00000504796.1:n.*489T>G
ENST00000678337.1:c.633T>G	ENSP00000504759.1:p.Asp211Glu
ENST00000678725.1:n.1574T>G
ENST00000679090.1:n.1182T>G
ENST00000679148.1:n.3559T>G
ENST00000679171.1:n.2958T>G
ENST00000679260.1:c.399+1819T>G	ENSP00000504534.1:n.399+1819T>G
ENST00000271651.7:c.597T>G	ENSP00000271651.3:p.Asp199Glu
ENST00000443913.1:c.774T>G	ENSP00000405083.1:p.Asp258Glu
ENST00000480670.1:n.437T>G
NM_000396.3:c.597T>G	NP_000387.1:p.Asp199Glu
NM_000396.4:c.597T>G MANE Select	NP_000387.1:p.Asp199Glu