Canonical Allele Identifier: CA342336687

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776662T>G (hg19) ; chr1:g.150804186T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804186T>G , CM000663.2:g.150804186T>G	GRCh38
NC_000001.10:g.150776662T>G , CM000663.1:g.150776662T>G	GRCh37
NC_000001.9:g.149043286T>G	NCBI36
NG_011848.1:g.9151A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.453A>C MANE Select	ENSP00000271651.3:p.Gln151His
ENST00000443913.2:c.630A>C	ENSP00000405083.2:p.Gln210His
ENST00000480670.2:n.3522A>C
ENST00000676680.1:c.453A>C	ENSP00000503270.1:p.Gln151His
ENST00000676716.1:c.330A>C	ENSP00000504737.1:p.Gln110His
ENST00000676751.1:c.453A>C	ENSP00000502964.1:p.Gln151His
ENST00000676824.1:c.453A>C	ENSP00000504176.1:p.Gln151His
ENST00000676966.1:c.453A>C	ENSP00000503723.1:p.Gln151His
ENST00000676970.1:c.453A>C	ENSP00000503832.1:p.Gln151His
ENST00000677330.1:n.2279A>C
ENST00000677611.1:n.305A>C
ENST00000677887.1:c.495A>C	ENSP00000503876.1:p.Gln165His
ENST00000678275.1:c.*345A>C	ENSP00000504796.1:n.*345A>C
ENST00000678337.1:c.489A>C	ENSP00000504759.1:p.Gln163His
ENST00000678725.1:n.1430A>C
ENST00000679090.1:n.1038A>C
ENST00000679148.1:n.3415A>C
ENST00000679171.1:n.2814A>C
ENST00000679260.1:c.399+1675A>C	ENSP00000504534.1:n.399+1675A>C
ENST00000271651.7:c.453A>C	ENSP00000271651.3:p.Gln151His
ENST00000443913.1:c.630A>C	ENSP00000405083.1:p.Gln210His
ENST00000480670.1:n.293A>C
NM_000396.3:c.453A>C	NP_000387.1:p.Gln151His
NM_000396.4:c.453A>C MANE Select	NP_000387.1:p.Gln151His