Canonical Allele Identifier: CA6168909

Gene: FOLR3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_000804.4:c.292C>T MANE Select	NP_000795.2:p.Arg98Cys
ENST00000611028.3:c.292C>T MANE Select	ENSP00000481114.1:p.Arg98Cys
NM_000804.2:c.292C>T	NP_000795.2:p.Arg98Cys
NM_000804.3:c.292C>T	NP_000795.2:p.Arg98Cys
NM_001318045.1:c.19C>T	NP_001304974.1:p.Arg7Cys
NM_001318045.2:c.19C>T	NP_001304974.1:p.Arg7Cys
ENST00000442948.3:c.286C>T	ENSP00000411161.3:p.Arg96Cys
ENST00000611028.2:c.292C>T	ENSP00000481114.1:p.Arg98Cys
ENST00000612844.4:c.420C>T	ENSP00000481027.1:p.Ser140=
ENST00000622388.4:c.292C>T	ENSP00000481833.1:p.Arg98Cys
XM_011544873.1:c.292C>T	XP_011543175.1:p.Arg98Cys
XM_011544874.1:c.292C>T	XP_011543176.1:p.Arg98Cys
XM_011544875.1:c.19C>T	XP_011543177.1:p.Arg7Cys
XM_011544876.1:c.81+24C>T	XP_011543178.1:n.81+24C>T