Canonical Allele Identifier: CA2647835935

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804360-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804360T>A , CM000663.2:g.150804360T>A	GRCh38
NC_000001.10:g.150776836T>A , CM000663.1:g.150776836T>A	GRCh37
NC_000001.9:g.149043460T>A	NCBI36
NG_011848.1:g.8977A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.400-121A>T MANE Select	ENSP00000271651.3:n.400-121A>T
ENST00000443913.2:c.577-121A>T	ENSP00000405083.2:n.577-121A>T
ENST00000480670.2:n.3469-121A>T
ENST00000676680.1:c.400-121A>T	ENSP00000503270.1:n.400-121A>T
ENST00000676716.1:c.277-121A>T	ENSP00000504737.1:n.277-121A>T
ENST00000676751.1:c.400-121A>T	ENSP00000502964.1:n.400-121A>T
ENST00000676824.1:c.400-121A>T	ENSP00000504176.1:n.400-121A>T
ENST00000676966.1:c.400-121A>T	ENSP00000503723.1:n.400-121A>T
ENST00000676970.1:c.400-121A>T	ENSP00000503832.1:n.400-121A>T
ENST00000677330.1:n.2226-121A>T
ENST00000677611.1:n.252-121A>T
ENST00000677887.1:c.442-121A>T	ENSP00000503876.1:n.442-121A>T
ENST00000678275.1:c.*292-121A>T	ENSP00000504796.1:n.*292-121A>T
ENST00000678337.1:c.436-121A>T	ENSP00000504759.1:n.436-121A>T
ENST00000678725.1:n.1377-121A>T
ENST00000679090.1:n.985-121A>T
ENST00000679148.1:n.3241A>T
ENST00000679171.1:n.2761-121A>T
ENST00000679260.1:c.399+1501A>T	ENSP00000504534.1:n.399+1501A>T
ENST00000271651.7:c.400-121A>T	ENSP00000271651.3:n.400-121A>T
ENST00000443913.1:c.577-121A>T	ENSP00000405083.1:n.577-121A>T
ENST00000480670.1:n.240-121A>T
NM_000396.3:c.400-121A>T	NP_000387.1:n.400-121A>T
NM_000396.4:c.400-121A>T MANE Select	NP_000387.1:n.400-121A>T