Canonical Allele Identifier: CA342336677

Gene: CTSK

Linked Data

• ClinVar Variation Id: 1949482
• ClinVar RCV Id: RCV002659471
• MyVariant Identifiers: chr1:g.150776658T>A (hg19) ; chr1:g.150804182T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804182T>A , CM000663.2:g.150804182T>A	GRCh38
NC_000001.10:g.150776658T>A , CM000663.1:g.150776658T>A	GRCh37
NC_000001.9:g.149043282T>A	NCBI36
NG_011848.1:g.9155A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.457A>T MANE Select	ENSP00000271651.3:p.Lys153Ter
ENST00000443913.2:c.634A>T	ENSP00000405083.2:p.Lys212Ter
ENST00000480670.2:n.3526A>T
ENST00000676680.1:c.457A>T	ENSP00000503270.1:p.Lys153Ter
ENST00000676716.1:c.334A>T	ENSP00000504737.1:p.Lys112Ter
ENST00000676751.1:c.457A>T	ENSP00000502964.1:p.Lys153Ter
ENST00000676824.1:c.457A>T	ENSP00000504176.1:p.Lys153Ter
ENST00000676966.1:c.457A>T	ENSP00000503723.1:p.Lys153Ter
ENST00000676970.1:c.457A>T	ENSP00000503832.1:p.Lys153Ter
ENST00000677330.1:n.2283A>T
ENST00000677611.1:n.309A>T
ENST00000677887.1:c.499A>T	ENSP00000503876.1:p.Lys167Ter
ENST00000678275.1:c.*349A>T	ENSP00000504796.1:n.*349A>T
ENST00000678337.1:c.493A>T	ENSP00000504759.1:p.Lys165Ter
ENST00000678725.1:n.1434A>T
ENST00000679090.1:n.1042A>T
ENST00000679148.1:n.3419A>T
ENST00000679171.1:n.2818A>T
ENST00000679260.1:c.399+1679A>T	ENSP00000504534.1:n.399+1679A>T
ENST00000271651.7:c.457A>T	ENSP00000271651.3:p.Lys153Ter
ENST00000443913.1:c.634A>T	ENSP00000405083.1:p.Lys212Ter
ENST00000480670.1:n.297A>T
NM_000396.3:c.457A>T	NP_000387.1:p.Lys153Ter
NM_000396.4:c.457A>T MANE Select	NP_000387.1:p.Lys153Ter