Canonical Allele Identifier: CA342337623

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806728C>T , CM000663.2:g.150806728C>T	GRCh38
NC_000001.10:g.150779204C>T , CM000663.1:g.150779204C>T	GRCh37
NC_000001.9:g.149045828C>T	NCBI36
NG_011848.1:g.6609G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.78G>A MANE Select	NP_000387.1:p.Trp26Ter
ENST00000271651.8:c.78G>A MANE Select	ENSP00000271651.3:p.Trp26Ter
NM_000396.3:c.78G>A	NP_000387.1:p.Trp26Ter
ENST00000271651.7:c.78G>A	ENSP00000271651.3:p.Trp26Ter
ENST00000443913.1:c.255G>A	ENSP00000405083.1:p.Trp85Ter
ENST00000443913.2:c.255G>A	ENSP00000405083.2:p.Trp85Ter
ENST00000480670.1:n.41G>A
ENST00000480670.2:n.2686G>A
ENST00000676680.1:c.78G>A	ENSP00000503270.1:p.Trp26Ter
ENST00000676716.1:c.78G>A	ENSP00000504737.1:p.Trp26Ter
ENST00000676751.1:c.78G>A	ENSP00000502964.1:p.Trp26Ter
ENST00000676824.1:c.78G>A	ENSP00000504176.1:p.Trp26Ter
ENST00000676966.1:c.78G>A	ENSP00000503723.1:p.Trp26Ter
ENST00000676970.1:c.78G>A	ENSP00000503832.1:p.Trp26Ter
ENST00000677330.1:n.1443G>A
ENST00000677887.1:c.120G>A	ENSP00000503876.1:p.Trp40Ter
ENST00000678275.1:c.78G>A	ENSP00000504796.1:p.Trp26Ter
ENST00000678337.1:c.114G>A	ENSP00000504759.1:p.Trp38Ter
ENST00000678725.1:n.1055G>A
ENST00000679090.1:n.202G>A
ENST00000679148.1:n.958G>A
ENST00000679171.1:n.1978G>A
ENST00000679260.1:c.78G>A	ENSP00000504534.1:p.Trp26Ter