Canonical Allele Identifier: CA420699488

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776686G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804210G>A , CM000663.2:g.150804210G>A	GRCh38
NC_000001.10:g.150776686G>A , CM000663.1:g.150776686G>A	GRCh37
NC_000001.9:g.149043310G>A	NCBI36
NG_011848.1:g.9127C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.429C>T MANE Select	ENSP00000271651.3:p.Ser143=
ENST00000443913.2:c.606C>T	ENSP00000405083.2:p.Ser202=
ENST00000480670.2:n.3498C>T
ENST00000676680.1:c.429C>T	ENSP00000503270.1:p.Ser143=
ENST00000676716.1:c.306C>T	ENSP00000504737.1:p.Ser102=
ENST00000676751.1:c.429C>T	ENSP00000502964.1:p.Ser143=
ENST00000676824.1:c.429C>T	ENSP00000504176.1:p.Ser143=
ENST00000676966.1:c.429C>T	ENSP00000503723.1:p.Ser143=
ENST00000676970.1:c.429C>T	ENSP00000503832.1:p.Ser143=
ENST00000677330.1:n.2255C>T
ENST00000677611.1:n.281C>T
ENST00000677887.1:c.471C>T	ENSP00000503876.1:p.Ser157=
ENST00000678275.1:c.*321C>T	ENSP00000504796.1:n.*321C>T
ENST00000678337.1:c.465C>T	ENSP00000504759.1:p.Ser155=
ENST00000678725.1:n.1406C>T
ENST00000679090.1:n.1014C>T
ENST00000679148.1:n.3391C>T
ENST00000679171.1:n.2790C>T
ENST00000679260.1:c.399+1651C>T	ENSP00000504534.1:n.399+1651C>T
ENST00000271651.7:c.429C>T	ENSP00000271651.3:p.Ser143=
ENST00000443913.1:c.606C>T	ENSP00000405083.1:p.Ser202=
ENST00000480670.1:n.269C>T
NM_000396.3:c.429C>T	NP_000387.1:p.Ser143=
NM_000396.4:c.429C>T MANE Select	NP_000387.1:p.Ser143=