Canonical Allele Identifier: CA1139656302

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806045T>C , CM000663.2:g.150806045T>C	GRCh38
NC_000001.10:g.150778521T>C , CM000663.1:g.150778521T>C	GRCh37
NC_000001.9:g.149045145T>C	NCBI36
NG_011848.1:g.7292A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.244-29A>G MANE Select	NP_000387.1:n.244-29A>G
ENST00000271651.8:c.244-29A>G MANE Select	ENSP00000271651.3:n.244-29A>G
NM_000396.3:c.244-29A>G	NP_000387.1:n.244-29A>G
ENST00000271651.7:c.244-29A>G	ENSP00000271651.3:n.244-29A>G
ENST00000443913.1:c.421-29A>G	ENSP00000405083.1:n.421-29A>G
ENST00000443913.2:c.421-29A>G	ENSP00000405083.2:n.421-29A>G
ENST00000480670.1:n.84-29A>G
ENST00000480670.2:n.3313-29A>G
ENST00000676680.1:c.244-29A>G	ENSP00000503270.1:n.244-29A>G
ENST00000676716.1:c.121-29A>G	ENSP00000504737.1:n.121-29A>G
ENST00000676751.1:c.244-29A>G	ENSP00000502964.1:n.244-29A>G
ENST00000676824.1:c.244-29A>G	ENSP00000504176.1:n.244-29A>G
ENST00000676966.1:c.244-29A>G	ENSP00000503723.1:n.244-29A>G
ENST00000676970.1:c.244-29A>G	ENSP00000503832.1:n.244-29A>G
ENST00000677330.1:n.2070-29A>G
ENST00000677611.1:n.67A>G
ENST00000677887.1:c.286-29A>G	ENSP00000503876.1:n.286-29A>G
ENST00000678275.1:c.*136-29A>G	ENSP00000504796.1:n.*136-29A>G
ENST00000678337.1:c.280-29A>G	ENSP00000504759.1:n.280-29A>G
ENST00000678725.1:n.1221-29A>G
ENST00000679090.1:n.829-29A>G
ENST00000679148.1:n.1585-29A>G
ENST00000679171.1:n.2605-29A>G
ENST00000679260.1:c.244-29A>G	ENSP00000504534.1:n.244-29A>G