Canonical Allele Identifier: CA342336605

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804149-G-A
• MyVariant Identifiers: chr1:g.150776625G>A (hg19) ; chr1:g.150804149G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804149G>A , CM000663.2:g.150804149G>A	GRCh38
NC_000001.10:g.150776625G>A , CM000663.1:g.150776625G>A	GRCh37
NC_000001.9:g.149043249G>A	NCBI36
NG_011848.1:g.9188C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.490C>T MANE Select	ENSP00000271651.3:p.Pro164Ser
ENST00000443913.2:c.667C>T	ENSP00000405083.2:p.Pro223Ser
ENST00000480670.2:n.3559C>T
ENST00000676680.1:c.490C>T	ENSP00000503270.1:p.Pro164Ser
ENST00000676716.1:c.367C>T	ENSP00000504737.1:p.Pro123Ser
ENST00000676751.1:c.490C>T	ENSP00000502964.1:p.Pro164Ser
ENST00000676824.1:c.490C>T	ENSP00000504176.1:p.Pro164Ser
ENST00000676966.1:c.490C>T	ENSP00000503723.1:p.Pro164Ser
ENST00000676970.1:c.490C>T	ENSP00000503832.1:p.Pro164Ser
ENST00000677330.1:n.2316C>T
ENST00000677611.1:n.342C>T
ENST00000677887.1:c.532C>T	ENSP00000503876.1:p.Pro178Ser
ENST00000678275.1:c.*382C>T	ENSP00000504796.1:n.*382C>T
ENST00000678337.1:c.526C>T	ENSP00000504759.1:p.Pro176Ser
ENST00000678725.1:n.1467C>T
ENST00000679090.1:n.1075C>T
ENST00000679148.1:n.3452C>T
ENST00000679171.1:n.2851C>T
ENST00000679260.1:c.399+1712C>T	ENSP00000504534.1:n.399+1712C>T
ENST00000271651.7:c.490C>T	ENSP00000271651.3:p.Pro164Ser
ENST00000443913.1:c.667C>T	ENSP00000405083.1:p.Pro223Ser
ENST00000480670.1:n.330C>T
NM_000396.3:c.490C>T	NP_000387.1:p.Pro164Ser
NM_000396.4:c.490C>T MANE Select	NP_000387.1:p.Pro164Ser