Canonical Allele Identifier: CA420701493

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779249C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806773C>A , CM000663.2:g.150806773C>A	GRCh38
NC_000001.10:g.150779249C>A , CM000663.1:g.150779249C>A	GRCh37
NC_000001.9:g.149045873C>A	NCBI36
NG_011848.1:g.6564G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.33G>T MANE Select	ENSP00000271651.3:p.Val11=
ENST00000443913.2:c.210G>T	ENSP00000405083.2:p.Val70=
ENST00000480670.2:n.2641G>T
ENST00000676680.1:c.33G>T	ENSP00000503270.1:p.Val11=
ENST00000676716.1:c.33G>T	ENSP00000504737.1:p.Val11=
ENST00000676751.1:c.33G>T	ENSP00000502964.1:p.Val11=
ENST00000676824.1:c.33G>T	ENSP00000504176.1:p.Val11=
ENST00000676966.1:c.33G>T	ENSP00000503723.1:p.Val11=
ENST00000676970.1:c.33G>T	ENSP00000503832.1:p.Val11=
ENST00000677330.1:n.1398G>T
ENST00000677887.1:c.75G>T	ENSP00000503876.1:p.Val25=
ENST00000678275.1:c.33G>T	ENSP00000504796.1:p.Val11=
ENST00000678337.1:c.69G>T	ENSP00000504759.1:p.Val23=
ENST00000678725.1:n.1010G>T
ENST00000679090.1:n.157G>T
ENST00000679148.1:n.913G>T
ENST00000679171.1:n.1933G>T
ENST00000679260.1:c.33G>T	ENSP00000504534.1:p.Val11=
ENST00000271651.7:c.33G>T	ENSP00000271651.3:p.Val11=
ENST00000443913.1:c.210G>T	ENSP00000405083.1:p.Val70=
NM_000396.3:c.33G>T	NP_000387.1:p.Val11=
NM_000396.4:c.33G>T MANE Select	NP_000387.1:p.Val11=