Canonical Allele Identifier: CA679926618

Gene: FOLR3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72138457C>T , CM000673.2:g.72138457C>T	GRCh38
NC_000011.9:g.71849503C>T , CM000673.1:g.71849503C>T	GRCh37
NC_000011.8:g.71527151C>T	NCBI36
NG_032935.1:g.7733C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000611028.3:c.169-504C>T MANE Select	ENSP00000481114.1:n.169-504C>T
ENST00000442948.3:c.163-504C>T	ENSP00000411161.3:n.163-504C>T
ENST00000546166.1:c.163-504C>T	ENSP00000446279.1:n.163-504C>T
ENST00000611028.2:c.169-504C>T	ENSP00000481114.1:n.169-504C>T
ENST00000612844.4:c.169-376C>T	ENSP00000481027.1:n.169-376C>T
ENST00000622388.4:c.169-504C>T	ENSP00000481833.1:n.169-504C>T
NM_000804.2:c.169-504C>T	NP_000795.2:n.169-504C>T
XM_011544873.1:c.169-504C>T	XP_011543175.1:n.169-504C>T
XM_011544874.1:c.169-504C>T	XP_011543176.1:n.169-504C>T
XM_011544875.1:c.-233-376C>T	XP_011543177.1:n.-233-376C>T
NM_000804.3:c.169-504C>T	NP_000795.2:n.169-504C>T
NM_001318045.1:c.-233-376C>T	NP_001304974.1:n.-233-376C>T
NM_000804.4:c.169-504C>T MANE Select	NP_000795.2:n.169-504C>T
NM_001318045.2:c.-233-376C>T	NP_001304974.1:n.-233-376C>T