Canonical Allele Identifier: CA2308732898
Community Standard Title: NM_002035.4(KDSR):c.557A= (p.Tyr186=)
Gene: KDSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63350940T= , CM000680.2:g.63350940T= GRCh38
NC_000018.9:g.61018173T= , CM000680.1:g.61018173T= GRCh37
NC_000018.8:g.59169153T= NCBI36
NG_028249.1:g.21334A=

Transcript Alleles

HGVS Amino-acid Change
NM_002035.4:c.557A= MANE Select NP_002026.1:p.Tyr186=
ENST00000645214.2:c.557A= MANE Select ENSP00000494352.1:p.Tyr186=
NM_002035.2:c.557A= NP_002026.1:p.Tyr186=
ENST00000326575.9:c.417+4264A= ENSP00000312939.5:n.417+4264A=
ENST00000406396.7:c.557A= ENSP00000385083.2:p.Tyr186=
ENST00000585750.1:n.251A=
ENST00000591902.5:c.272A= ENSP00000468203.1:p.Tyr91=
ENST00000591902.6:c.557A= ENSP00000468203.2:p.Tyr186=
ENST00000644624.1:c.*496A= ENSP00000494878.1:n.*496A=
ENST00000646205.1:c.*707A= ENSP00000496260.1:n.*707A=
XM_005266677.1:c.557A= XP_005266734.1:p.Tyr186=
XM_005266677.3:c.557A= XP_005266734.1:p.Tyr186=
XM_006722433.2:c.470A= XP_006722496.1:p.Tyr157=
XM_017025690.2:c.326A= XP_016881179.1:p.Tyr109=