Canonical Allele Identifier: CA2580084845

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 2094116
• ClinVar RCV Id: RCV002996978

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195367_72195369delinsAGA , CM000673.2:g.72195367_72195369delinsAGA	GRCh38
NC_000011.9:g.71906411_71906413delinsAGA , CM000673.1:g.71906411_71906413delinsAGA	GRCh37
NC_000011.8:g.71584059_71584061delinsAGA	NCBI36
NG_015863.1:g.10810_10812delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.265_267delinsAGA	ENSP00000308137.4:p.Cys89Arg
ENST00000393676.5:c.265_267delinsAGA MANE Select	ENSP00000377281.3:p.Cys89Arg
ENST00000675784.1:c.265_267delinsAGA	ENSP00000502440.1:p.Cys89Arg
ENST00000312293.8:c.265_267delinsAGA	ENSP00000308137.4:p.Cys89Arg
ENST00000393676.3:c.265_267delinsAGA	ENSP00000377281.3:p.Cys89Arg
ENST00000393679.5:c.265_267delinsAGA	ENSP00000377284.1:p.Cys89Arg
ENST00000393681.6:c.265_267delinsAGA	ENSP00000377286.2:p.Cys89Arg
NM_000802.3:c.265_267delinsAGA	NP_000793.1:p.Cys89Arg
NM_016724.2:c.265_267delinsAGA	NP_057936.1:p.Cys89Arg
NM_016725.2:c.265_267delinsAGA	NP_057937.1:p.Cys89Arg
NM_016729.2:c.265_267delinsAGA	NP_057941.1:p.Cys89Arg
NM_016729.3:c.265_267delinsAGA MANE Select	NP_057941.1:p.Cys89Arg
NM_016724.3:c.265_267delinsAGA	NP_057936.1:p.Cys89Arg
NM_016725.3:c.265_267delinsAGA	NP_057937.1:p.Cys89Arg