Canonical Allele Identifier: CA1630855222
Gene: FOLR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72139084C= , CM000673.2:g.72139084C= GRCh38
NC_000011.9:g.71850130C= , CM000673.1:g.71850130C= GRCh37
NC_000011.8:g.71527778C= NCBI36
NG_032935.1:g.8360C=

Transcript Alleles

HGVS Amino-acid Change
NM_000804.4:c.292C= MANE Select NP_000795.2:p.Arg98=
ENST00000611028.3:c.292C= MANE Select ENSP00000481114.1:p.Arg98=
NM_000804.2:c.292C= NP_000795.2:p.Arg98=
NM_000804.3:c.292C= NP_000795.2:p.Arg98=
NM_001318045.1:c.19C= NP_001304974.1:p.Arg7=
NM_001318045.2:c.19C= NP_001304974.1:p.Arg7=
ENST00000442948.3:c.286C= ENSP00000411161.3:p.Arg96=
ENST00000611028.2:c.292C= ENSP00000481114.1:p.Arg98=
ENST00000612844.4:c.420C= ENSP00000481027.1:p.Ser140=
ENST00000622388.4:c.292C= ENSP00000481833.1:p.Arg98=
XM_011544873.1:c.292C= XP_011543175.1:p.Arg98=
XM_011544874.1:c.292C= XP_011543176.1:p.Arg98=
XM_011544875.1:c.19C= XP_011543177.1:p.Arg7=
XM_011544876.1:c.81+24C= XP_011543178.1:n.81+24C=