Canonical Allele Identifier: CA1981892137

Gene: FOLR2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218597T= , CM000673.2:g.72218597T=	GRCh38
NC_000011.9:g.71929641T= , CM000673.1:g.71929641T=	GRCh37
NC_000011.8:g.71607289T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000298223.11:c.13T= MANE Select	ENSP00000298223.6:p.Trp5=
ENST00000298223.10:c.13T=	ENSP00000298223.6:p.Trp5=
ENST00000321324.11:c.52T=	ENSP00000321957.7:p.Trp18=
ENST00000449475.6:c.64T=	ENSP00000405638.2:p.Trp22=
ENST00000454954.6:c.27+1672T=	ENSP00000414094.2:n.27+1672T=
ENST00000535625.5:c.13T=	ENSP00000444794.1:p.Trp5=
ENST00000536778.5:c.58T=	ENSP00000438568.1:p.Trp20=
ENST00000538353.1:c.13T=	ENSP00000440337.1:p.Trp5=
ENST00000539412.5:c.46T=	ENSP00000441547.1:p.Trp16=
ENST00000541003.5:c.151T=	ENSP00000443307.1:p.Trp51=
ENST00000619261.4:c.64T=	ENSP00000480592.1:p.Trp22=
NM_000803.4:c.13T=	NP_000794.3:p.Trp5=
NM_001113534.1:c.13T=	NP_001107006.1:p.Trp5=
NM_001113535.1:c.13T=	NP_001107007.1:p.Trp5=
NM_001113536.1:c.13T=	NP_001107008.1:p.Trp5=
XM_005273856.2:c.40T=	XP_005273913.1:p.Trp14=
XM_011544869.1:c.64T=	XP_011543171.1:p.Trp22=
XM_011544870.1:c.58T=	XP_011543172.1:p.Trp20=
XM_011544871.1:c.52T=	XP_011543173.1:p.Trp18=
XM_011544872.1:c.46T=	XP_011543174.1:p.Trp16=
XM_005273856.4:c.40T=	XP_005273913.1:p.Trp14=
XM_024448412.1:c.64T=	XP_024304180.1:p.Trp22=
NM_000803.5:c.13T= MANE Select	NP_000794.3:p.Trp5=
NM_001113534.2:c.13T=	NP_001107006.1:p.Trp5=
NM_001113535.2:c.13T=	NP_001107007.1:p.Trp5=
NM_001113536.2:c.13T=	NP_001107008.1:p.Trp5=