Canonical Allele Identifier: CA1981879971

Gene: FOLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195454C= , CM000673.2:g.72195454C=	GRCh38
NC_000011.9:g.71906498C= , CM000673.1:g.71906498C=	GRCh37
NC_000011.8:g.71584146C=	NCBI36
NG_015863.1:g.10897C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016729.3:c.352C= MANE Select	NP_057941.1:p.Gln118=
ENST00000393676.5:c.352C= MANE Select	ENSP00000377281.3:p.Gln118=
NM_000802.3:c.352C=	NP_000793.1:p.Gln118=
NM_016724.2:c.352C=	NP_057936.1:p.Gln118=
NM_016724.3:c.352C=	NP_057936.1:p.Gln118=
NM_016725.2:c.352C=	NP_057937.1:p.Gln118=
NM_016725.3:c.352C=	NP_057937.1:p.Gln118=
NM_016729.2:c.352C=	NP_057941.1:p.Gln118=
ENST00000312293.8:c.352C=	ENSP00000308137.4:p.Gln118=
ENST00000312293.9:c.352C=	ENSP00000308137.4:p.Gln118=
ENST00000393676.3:c.352C=	ENSP00000377281.3:p.Gln118=
ENST00000393679.5:c.352C=	ENSP00000377284.1:p.Gln118=
ENST00000393681.6:c.352C=	ENSP00000377286.2:p.Gln118=
ENST00000675784.1:c.352C=	ENSP00000502440.1:p.Gln118=