Canonical Allele Identifier: CA342336480

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804093-C-A
• MyVariant Identifiers: chr1:g.150776569C>A (hg19) ; chr1:g.150804093C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804093C>A , CM000663.2:g.150804093C>A	GRCh38
NC_000001.10:g.150776569C>A , CM000663.1:g.150776569C>A	GRCh37
NC_000001.9:g.149043193C>A	NCBI36
NG_011848.1:g.9244G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.546G>T MANE Select	ENSP00000271651.3:p.Met182Ile
ENST00000443913.2:c.723G>T	ENSP00000405083.2:p.Met241Ile
ENST00000480670.2:n.3615G>T
ENST00000676680.1:c.546G>T	ENSP00000503270.1:p.Met182Ile
ENST00000676716.1:c.423G>T	ENSP00000504737.1:p.Met141Ile
ENST00000676751.1:c.546G>T	ENSP00000502964.1:p.Met182Ile
ENST00000676824.1:c.546G>T	ENSP00000504176.1:p.Met182Ile
ENST00000676966.1:c.546G>T	ENSP00000503723.1:p.Met182Ile
ENST00000676970.1:c.546G>T	ENSP00000503832.1:p.Met182Ile
ENST00000677330.1:n.2372G>T
ENST00000677611.1:n.398G>T
ENST00000677887.1:c.588G>T	ENSP00000503876.1:p.Met196Ile
ENST00000678275.1:c.*438G>T	ENSP00000504796.1:n.*438G>T
ENST00000678337.1:c.582G>T	ENSP00000504759.1:p.Met194Ile
ENST00000678725.1:n.1523G>T
ENST00000679090.1:n.1131G>T
ENST00000679148.1:n.3508G>T
ENST00000679171.1:n.2907G>T
ENST00000679260.1:c.399+1768G>T	ENSP00000504534.1:n.399+1768G>T
ENST00000271651.7:c.546G>T	ENSP00000271651.3:p.Met182Ile
ENST00000443913.1:c.723G>T	ENSP00000405083.1:p.Met241Ile
ENST00000480670.1:n.386G>T
NM_000396.3:c.546G>T	NP_000387.1:p.Met182Ile
NM_000396.4:c.546G>T MANE Select	NP_000387.1:p.Met182Ile