Canonical Allele Identifier: CA2647835904

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804303-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804303C>T , CM000663.2:g.150804303C>T	GRCh38
NC_000001.10:g.150776779C>T , CM000663.1:g.150776779C>T	GRCh37
NC_000001.9:g.149043403C>T	NCBI36
NG_011848.1:g.9034G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.400-64G>A MANE Select	ENSP00000271651.3:n.400-64G>A
ENST00000443913.2:c.577-64G>A	ENSP00000405083.2:n.577-64G>A
ENST00000480670.2:n.3469-64G>A
ENST00000676680.1:c.400-64G>A	ENSP00000503270.1:n.400-64G>A
ENST00000676716.1:c.277-64G>A	ENSP00000504737.1:n.277-64G>A
ENST00000676751.1:c.400-64G>A	ENSP00000502964.1:n.400-64G>A
ENST00000676824.1:c.400-64G>A	ENSP00000504176.1:n.400-64G>A
ENST00000676966.1:c.400-64G>A	ENSP00000503723.1:n.400-64G>A
ENST00000676970.1:c.400-64G>A	ENSP00000503832.1:n.400-64G>A
ENST00000677330.1:n.2226-64G>A
ENST00000677611.1:n.252-64G>A
ENST00000677887.1:c.442-64G>A	ENSP00000503876.1:n.442-64G>A
ENST00000678275.1:c.*292-64G>A	ENSP00000504796.1:n.*292-64G>A
ENST00000678337.1:c.436-64G>A	ENSP00000504759.1:n.436-64G>A
ENST00000678725.1:n.1377-64G>A
ENST00000679090.1:n.985-64G>A
ENST00000679148.1:n.3298G>A
ENST00000679171.1:n.2761-64G>A
ENST00000679260.1:c.399+1558G>A	ENSP00000504534.1:n.399+1558G>A
ENST00000271651.7:c.400-64G>A	ENSP00000271651.3:n.400-64G>A
ENST00000443913.1:c.577-64G>A	ENSP00000405083.1:n.577-64G>A
ENST00000480670.1:n.240-64G>A
NM_000396.3:c.400-64G>A	NP_000387.1:n.400-64G>A
NM_000396.4:c.400-64G>A MANE Select	NP_000387.1:n.400-64G>A