Canonical Allele Identifier: CA420699479

Gene: CTSK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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