Canonical Allele Identifier: CA2479314202

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804088T= , CM000663.2:g.150804088T=	GRCh38
NC_000001.10:g.150776564T= , CM000663.1:g.150776564T=	GRCh37
NC_000001.9:g.149043188T=	NCBI36
NG_011848.1:g.9249A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.551A= MANE Select	ENSP00000271651.3:p.Asn184=
ENST00000443913.2:c.728A=	ENSP00000405083.2:p.Asn243=
ENST00000480670.2:n.3620A=
ENST00000676680.1:c.551A=	ENSP00000503270.1:p.Asn184=
ENST00000676716.1:c.428A=	ENSP00000504737.1:p.Asn143=
ENST00000676751.1:c.551A=	ENSP00000502964.1:p.Asn184=
ENST00000676824.1:c.551A=	ENSP00000504176.1:p.Asn184=
ENST00000676966.1:c.551A=	ENSP00000503723.1:p.Asn184=
ENST00000676970.1:c.551A=	ENSP00000503832.1:p.Asn184=
ENST00000677330.1:n.2377A=
ENST00000677611.1:n.403A=
ENST00000677887.1:c.593A=	ENSP00000503876.1:p.Asn198=
ENST00000678275.1:c.*443A=	ENSP00000504796.1:n.*443A=
ENST00000678337.1:c.587A=	ENSP00000504759.1:p.Asn196=
ENST00000678725.1:n.1528A=
ENST00000679090.1:n.1136A=
ENST00000679148.1:n.3513A=
ENST00000679171.1:n.2912A=
ENST00000679260.1:c.399+1773A=	ENSP00000504534.1:n.399+1773A=
ENST00000271651.7:c.551A=	ENSP00000271651.3:p.Asn184=
ENST00000443913.1:c.728A=	ENSP00000405083.1:p.Asn243=
ENST00000480670.1:n.391A=
NM_000396.3:c.551A=	NP_000387.1:p.Asn184=
NM_000396.4:c.551A= MANE Select	NP_000387.1:p.Asn184=