Canonical Allele Identifier: CA342336536

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776594T>C (hg19) ; chr1:g.150804118T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804118T>C , CM000663.2:g.150804118T>C	GRCh38
NC_000001.10:g.150776594T>C , CM000663.1:g.150776594T>C	GRCh37
NC_000001.9:g.149043218T>C	NCBI36
NG_011848.1:g.9219A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.521A>G MANE Select	ENSP00000271651.3:p.Asn174Ser
ENST00000443913.2:c.698A>G	ENSP00000405083.2:p.Asn233Ser
ENST00000480670.2:n.3590A>G
ENST00000676680.1:c.521A>G	ENSP00000503270.1:p.Asn174Ser
ENST00000676716.1:c.398A>G	ENSP00000504737.1:p.Asn133Ser
ENST00000676751.1:c.521A>G	ENSP00000502964.1:p.Asn174Ser
ENST00000676824.1:c.521A>G	ENSP00000504176.1:p.Asn174Ser
ENST00000676966.1:c.521A>G	ENSP00000503723.1:p.Asn174Ser
ENST00000676970.1:c.521A>G	ENSP00000503832.1:p.Asn174Ser
ENST00000677330.1:n.2347A>G
ENST00000677611.1:n.373A>G
ENST00000677887.1:c.563A>G	ENSP00000503876.1:p.Asn188Ser
ENST00000678275.1:c.*413A>G	ENSP00000504796.1:n.*413A>G
ENST00000678337.1:c.557A>G	ENSP00000504759.1:p.Asn186Ser
ENST00000678725.1:n.1498A>G
ENST00000679090.1:n.1106A>G
ENST00000679148.1:n.3483A>G
ENST00000679171.1:n.2882A>G
ENST00000679260.1:c.399+1743A>G	ENSP00000504534.1:n.399+1743A>G
ENST00000271651.7:c.521A>G	ENSP00000271651.3:p.Asn174Ser
ENST00000443913.1:c.698A>G	ENSP00000405083.1:p.Asn233Ser
ENST00000480670.1:n.361A>G
NM_000396.3:c.521A>G	NP_000387.1:p.Asn174Ser
NM_000396.4:c.521A>G MANE Select	NP_000387.1:p.Asn174Ser