Canonical Allele Identifier: CA1981880135

Gene: FOLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195860G= , CM000673.2:g.72195860G=	GRCh38
NC_000011.9:g.71906904G= , CM000673.1:g.71906904G=	GRCh37
NC_000011.8:g.71584552G=	NCBI36
NG_015863.1:g.11303G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000312293.9:c.494-37G=	ENSP00000308137.4:n.494-37G=
ENST00000393676.5:c.494-37G= MANE Select	ENSP00000377281.3:n.494-37G=
ENST00000675784.1:c.494-37G=	ENSP00000502440.1:n.494-37G=
ENST00000312293.8:c.494-37G=	ENSP00000308137.4:n.494-37G=
ENST00000393676.3:c.494-37G=	ENSP00000377281.3:n.494-37G=
ENST00000393679.5:c.494-37G=	ENSP00000377284.1:n.494-37G=
ENST00000393681.6:c.494-37G=	ENSP00000377286.2:n.494-37G=
NM_000802.3:c.494-37G=	NP_000793.1:n.494-37G=
NM_016724.2:c.494-37G=	NP_057936.1:n.494-37G=
NM_016725.2:c.494-37G=	NP_057937.1:n.494-37G=
NM_016729.2:c.494-37G=	NP_057941.1:n.494-37G=
NM_016729.3:c.494-37G= MANE Select	NP_057941.1:n.494-37G=
NM_016724.3:c.494-37G=	NP_057936.1:n.494-37G=
NM_016725.3:c.494-37G=	NP_057937.1:n.494-37G=