Canonical Allele Identifier: CA2647835936

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804361-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804361G>A , CM000663.2:g.150804361G>A	GRCh38
NC_000001.10:g.150776837G>A , CM000663.1:g.150776837G>A	GRCh37
NC_000001.9:g.149043461G>A	NCBI36
NG_011848.1:g.8976C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.400-122C>T MANE Select	ENSP00000271651.3:n.400-122C>T
ENST00000443913.2:c.577-122C>T	ENSP00000405083.2:n.577-122C>T
ENST00000480670.2:n.3469-122C>T
ENST00000676680.1:c.400-122C>T	ENSP00000503270.1:n.400-122C>T
ENST00000676716.1:c.277-122C>T	ENSP00000504737.1:n.277-122C>T
ENST00000676751.1:c.400-122C>T	ENSP00000502964.1:n.400-122C>T
ENST00000676824.1:c.400-122C>T	ENSP00000504176.1:n.400-122C>T
ENST00000676966.1:c.400-122C>T	ENSP00000503723.1:n.400-122C>T
ENST00000676970.1:c.400-122C>T	ENSP00000503832.1:n.400-122C>T
ENST00000677330.1:n.2226-122C>T
ENST00000677611.1:n.252-122C>T
ENST00000677887.1:c.442-122C>T	ENSP00000503876.1:n.442-122C>T
ENST00000678275.1:c.*292-122C>T	ENSP00000504796.1:n.*292-122C>T
ENST00000678337.1:c.436-122C>T	ENSP00000504759.1:n.436-122C>T
ENST00000678725.1:n.1377-122C>T
ENST00000679090.1:n.985-122C>T
ENST00000679148.1:n.3240C>T
ENST00000679171.1:n.2761-122C>T
ENST00000679260.1:c.399+1500C>T	ENSP00000504534.1:n.399+1500C>T
ENST00000271651.7:c.400-122C>T	ENSP00000271651.3:n.400-122C>T
ENST00000443913.1:c.577-122C>T	ENSP00000405083.1:n.577-122C>T
ENST00000480670.1:n.240-122C>T
NM_000396.3:c.400-122C>T	NP_000387.1:n.400-122C>T
NM_000396.4:c.400-122C>T MANE Select	NP_000387.1:n.400-122C>T