Canonical Allele Identifier: CA342337715

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779245T>A (hg19) ; chr1:g.150806769T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806769T>A , CM000663.2:g.150806769T>A	GRCh38
NC_000001.10:g.150779245T>A , CM000663.1:g.150779245T>A	GRCh37
NC_000001.9:g.149045869T>A	NCBI36
NG_011848.1:g.6568A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.37A>T MANE Select	ENSP00000271651.3:p.Ser13Cys
ENST00000443913.2:c.214A>T	ENSP00000405083.2:p.Ser72Cys
ENST00000480670.2:n.2645A>T
ENST00000676680.1:c.37A>T	ENSP00000503270.1:p.Ser13Cys
ENST00000676716.1:c.37A>T	ENSP00000504737.1:p.Ser13Cys
ENST00000676751.1:c.37A>T	ENSP00000502964.1:p.Ser13Cys
ENST00000676824.1:c.37A>T	ENSP00000504176.1:p.Ser13Cys
ENST00000676966.1:c.37A>T	ENSP00000503723.1:p.Ser13Cys
ENST00000676970.1:c.37A>T	ENSP00000503832.1:p.Ser13Cys
ENST00000677330.1:n.1402A>T
ENST00000677887.1:c.79A>T	ENSP00000503876.1:p.Ser27Cys
ENST00000678275.1:c.37A>T	ENSP00000504796.1:p.Ser13Cys
ENST00000678337.1:c.73A>T	ENSP00000504759.1:p.Ser25Cys
ENST00000678725.1:n.1014A>T
ENST00000679090.1:n.161A>T
ENST00000679148.1:n.917A>T
ENST00000679171.1:n.1937A>T
ENST00000679260.1:c.37A>T	ENSP00000504534.1:p.Ser13Cys
ENST00000271651.7:c.37A>T	ENSP00000271651.3:p.Ser13Cys
ENST00000443913.1:c.214A>T	ENSP00000405083.1:p.Ser72Cys
NM_000396.3:c.37A>T	NP_000387.1:p.Ser13Cys
NM_000396.4:c.37A>T MANE Select	NP_000387.1:p.Ser13Cys