Canonical Allele Identifier: CA1981892164

Gene: FOLR2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218659T= , CM000673.2:g.72218659T=	GRCh38
NC_000011.9:g.71929703T= , CM000673.1:g.71929703T=	GRCh37
NC_000011.8:g.71607351T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298223.11:c.75T= MANE Select	ENSP00000298223.6:p.Thr25=
ENST00000298223.10:c.75T=	ENSP00000298223.6:p.Thr25=
ENST00000321324.11:c.114T=	ENSP00000321957.7:p.Thr38=
ENST00000449475.6:c.126T=	ENSP00000405638.2:p.Thr42=
ENST00000454954.6:c.27+1734T=	ENSP00000414094.2:n.27+1734T=
ENST00000535625.5:c.75T=	ENSP00000444794.1:p.Thr25=
ENST00000536778.5:c.120T=	ENSP00000438568.1:p.Thr40=
ENST00000538353.1:c.75T=	ENSP00000440337.1:p.Thr25=
ENST00000539412.5:c.108T=	ENSP00000441547.1:p.Thr36=
ENST00000541003.5:c.213T=	ENSP00000443307.1:p.Thr71=
ENST00000619261.4:c.126T=	ENSP00000480592.1:p.Thr42=
NM_000803.4:c.75T=	NP_000794.3:p.Thr25=
NM_001113534.1:c.75T=	NP_001107006.1:p.Thr25=
NM_001113535.1:c.75T=	NP_001107007.1:p.Thr25=
NM_001113536.1:c.75T=	NP_001107008.1:p.Thr25=
XM_005273856.2:c.102T=	XP_005273913.1:p.Thr34=
XM_011544869.1:c.126T=	XP_011543171.1:p.Thr42=
XM_011544870.1:c.120T=	XP_011543172.1:p.Thr40=
XM_011544871.1:c.114T=	XP_011543173.1:p.Thr38=
XM_011544872.1:c.108T=	XP_011543174.1:p.Thr36=
XM_005273856.4:c.102T=	XP_005273913.1:p.Thr34=
XM_024448412.1:c.126T=	XP_024304180.1:p.Thr42=
NM_000803.5:c.75T= MANE Select	NP_000794.3:p.Thr25=
NM_001113534.2:c.75T=	NP_001107006.1:p.Thr25=
NM_001113535.2:c.75T=	NP_001107007.1:p.Thr25=
NM_001113536.2:c.75T=	NP_001107008.1:p.Thr25=