Canonical Allele Identifier: CA420699425

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804111-G-A
• MyVariant Identifiers: chr1:g.150776587G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804111G>A , CM000663.2:g.150804111G>A	GRCh38
NC_000001.10:g.150776587G>A , CM000663.1:g.150776587G>A	GRCh37
NC_000001.9:g.149043211G>A	NCBI36
NG_011848.1:g.9226C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.528C>T MANE Select	ENSP00000271651.3:p.Gly176=
ENST00000443913.2:c.705C>T	ENSP00000405083.2:p.Gly235=
ENST00000480670.2:n.3597C>T
ENST00000676680.1:c.528C>T	ENSP00000503270.1:p.Gly176=
ENST00000676716.1:c.405C>T	ENSP00000504737.1:p.Gly135=
ENST00000676751.1:c.528C>T	ENSP00000502964.1:p.Gly176=
ENST00000676824.1:c.528C>T	ENSP00000504176.1:p.Gly176=
ENST00000676966.1:c.528C>T	ENSP00000503723.1:p.Gly176=
ENST00000676970.1:c.528C>T	ENSP00000503832.1:p.Gly176=
ENST00000677330.1:n.2354C>T
ENST00000677611.1:n.380C>T
ENST00000677887.1:c.570C>T	ENSP00000503876.1:p.Gly190=
ENST00000678275.1:c.*420C>T	ENSP00000504796.1:n.*420C>T
ENST00000678337.1:c.564C>T	ENSP00000504759.1:p.Gly188=
ENST00000678725.1:n.1505C>T
ENST00000679090.1:n.1113C>T
ENST00000679148.1:n.3490C>T
ENST00000679171.1:n.2889C>T
ENST00000679260.1:c.399+1750C>T	ENSP00000504534.1:n.399+1750C>T
ENST00000271651.7:c.528C>T	ENSP00000271651.3:p.Gly176=
ENST00000443913.1:c.705C>T	ENSP00000405083.1:p.Gly235=
ENST00000480670.1:n.368C>T
NM_000396.3:c.528C>T	NP_000387.1:p.Gly176=
NM_000396.4:c.528C>T MANE Select	NP_000387.1:p.Gly176=