Canonical Allele Identifier: CA2308734772
Gene: KDSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63355481T= , CM000680.2:g.63355481T= GRCh38
NC_000018.9:g.61022714T= , CM000680.1:g.61022714T= GRCh37
NC_000018.8:g.59173694T= NCBI36
NG_028249.1:g.16793A=

Transcript Alleles

HGVS Amino-acid change
ENST00000591902.6:c.321+17A= ENSP00000468203.2:n.321+17A=
ENST00000644624.1:c.*260+17A= ENSP00000494878.1:n.*260+17A=
ENST00000645214.2:c.321+17A= MANE Select ENSP00000494352.1:n.321+17A=
ENST00000646205.1:c.*471+17A= ENSP00000496260.1:n.*471+17A=
ENST00000326575.9:c.321+17A= ENSP00000312939.5:n.321+17A=
ENST00000406396.7:c.321+17A= ENSP00000385083.2:n.321+17A=
ENST00000585750.1:n.17+17A=
ENST00000589530.5:n.423A=
ENST00000591902.5:c.36+17A= ENSP00000468203.1:n.36+17A=
ENST00000592327.1:c.321+17A= ENSP00000467962.1:n.321+17A=
NM_002035.2:c.321+17A= NP_002026.1:n.321+17A=
XM_005266677.1:c.321+17A= XP_005266734.1:n.321+17A=
XM_006722433.2:c.234+17A= XP_006722496.1:n.234+17A=
NM_002035.4:c.321+17A= MANE Select NP_002026.1:n.321+17A=
XM_005266677.3:c.321+17A= XP_005266734.1:n.321+17A=
XM_017025690.2:c.90+17A= XP_016881179.1:n.90+17A=