Canonical Allele Identifier: CA342336353

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776511G>T (hg19) ; chr1:g.150804035G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804035G>T , CM000663.2:g.150804035G>T	GRCh38
NC_000001.10:g.150776511G>T , CM000663.1:g.150776511G>T	GRCh37
NC_000001.9:g.149043135G>T	NCBI36
NG_011848.1:g.9302C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.604C>A MANE Select	ENSP00000271651.3:p.Pro202Thr
ENST00000443913.2:c.781C>A	ENSP00000405083.2:p.Pro261Thr
ENST00000480670.2:n.3673C>A
ENST00000676680.1:c.604C>A	ENSP00000503270.1:p.Pro202Thr
ENST00000676716.1:c.481C>A	ENSP00000504737.1:p.Pro161Thr
ENST00000676751.1:c.604C>A	ENSP00000502964.1:p.Pro202Thr
ENST00000676824.1:c.604C>A	ENSP00000504176.1:p.Pro202Thr
ENST00000676966.1:c.604C>A	ENSP00000503723.1:p.Pro202Thr
ENST00000676970.1:c.604C>A	ENSP00000503832.1:p.Pro202Thr
ENST00000677330.1:n.2430C>A
ENST00000677611.1:n.456C>A
ENST00000677887.1:c.646C>A	ENSP00000503876.1:p.Pro216Thr
ENST00000678275.1:c.*496C>A	ENSP00000504796.1:n.*496C>A
ENST00000678337.1:c.640C>A	ENSP00000504759.1:p.Pro214Thr
ENST00000678725.1:n.1581C>A
ENST00000679090.1:n.1189C>A
ENST00000679148.1:n.3566C>A
ENST00000679171.1:n.2965C>A
ENST00000679260.1:c.399+1826C>A	ENSP00000504534.1:n.399+1826C>A
ENST00000271651.7:c.604C>A	ENSP00000271651.3:p.Pro202Thr
ENST00000480670.1:n.444C>A
NM_000396.3:c.604C>A	NP_000387.1:p.Pro202Thr
NM_000396.4:c.604C>A MANE Select	NP_000387.1:p.Pro202Thr