Canonical Allele Identifier: CA420699478

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776674G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804198G>C , CM000663.2:g.150804198G>C	GRCh38
NC_000001.10:g.150776674G>C , CM000663.1:g.150776674G>C	GRCh37
NC_000001.9:g.149043298G>C	NCBI36
NG_011848.1:g.9139C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.441C>G MANE Select	ENSP00000271651.3:p.Ala147=
ENST00000443913.2:c.618C>G	ENSP00000405083.2:p.Ala206=
ENST00000480670.2:n.3510C>G
ENST00000676680.1:c.441C>G	ENSP00000503270.1:p.Ala147=
ENST00000676716.1:c.318C>G	ENSP00000504737.1:p.Ala106=
ENST00000676751.1:c.441C>G	ENSP00000502964.1:p.Ala147=
ENST00000676824.1:c.441C>G	ENSP00000504176.1:p.Ala147=
ENST00000676966.1:c.441C>G	ENSP00000503723.1:p.Ala147=
ENST00000676970.1:c.441C>G	ENSP00000503832.1:p.Ala147=
ENST00000677330.1:n.2267C>G
ENST00000677611.1:n.293C>G
ENST00000677887.1:c.483C>G	ENSP00000503876.1:p.Ala161=
ENST00000678275.1:c.*333C>G	ENSP00000504796.1:n.*333C>G
ENST00000678337.1:c.477C>G	ENSP00000504759.1:p.Ala159=
ENST00000678725.1:n.1418C>G
ENST00000679090.1:n.1026C>G
ENST00000679148.1:n.3403C>G
ENST00000679171.1:n.2802C>G
ENST00000679260.1:c.399+1663C>G	ENSP00000504534.1:n.399+1663C>G
ENST00000271651.7:c.441C>G	ENSP00000271651.3:p.Ala147=
ENST00000443913.1:c.618C>G	ENSP00000405083.1:p.Ala206=
ENST00000480670.1:n.281C>G
NM_000396.3:c.441C>G	NP_000387.1:p.Ala147=
NM_000396.4:c.441C>G MANE Select	NP_000387.1:p.Ala147=