Canonical Allele Identifier: CA420699468

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776659G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804183G>T , CM000663.2:g.150804183G>T	GRCh38
NC_000001.10:g.150776659G>T , CM000663.1:g.150776659G>T	GRCh37
NC_000001.9:g.149043283G>T	NCBI36
NG_011848.1:g.9154C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.456C>A MANE Select	ENSP00000271651.3:p.Leu152=
ENST00000443913.2:c.633C>A	ENSP00000405083.2:p.Leu211=
ENST00000480670.2:n.3525C>A
ENST00000676680.1:c.456C>A	ENSP00000503270.1:p.Leu152=
ENST00000676716.1:c.333C>A	ENSP00000504737.1:p.Leu111=
ENST00000676751.1:c.456C>A	ENSP00000502964.1:p.Leu152=
ENST00000676824.1:c.456C>A	ENSP00000504176.1:p.Leu152=
ENST00000676966.1:c.456C>A	ENSP00000503723.1:p.Leu152=
ENST00000676970.1:c.456C>A	ENSP00000503832.1:p.Leu152=
ENST00000677330.1:n.2282C>A
ENST00000677611.1:n.308C>A
ENST00000677887.1:c.498C>A	ENSP00000503876.1:p.Leu166=
ENST00000678275.1:c.*348C>A	ENSP00000504796.1:n.*348C>A
ENST00000678337.1:c.492C>A	ENSP00000504759.1:p.Leu164=
ENST00000678725.1:n.1433C>A
ENST00000679090.1:n.1041C>A
ENST00000679148.1:n.3418C>A
ENST00000679171.1:n.2817C>A
ENST00000679260.1:c.399+1678C>A	ENSP00000504534.1:n.399+1678C>A
ENST00000271651.7:c.456C>A	ENSP00000271651.3:p.Leu152=
ENST00000443913.1:c.633C>A	ENSP00000405083.1:p.Leu211=
ENST00000480670.1:n.296C>A
NM_000396.3:c.456C>A	NP_000387.1:p.Leu152=
NM_000396.4:c.456C>A MANE Select	NP_000387.1:p.Leu152=