Canonical Allele Identifier: CA1139662086

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 937092
• ClinVar RCV Id: RCV001206040
• dbSNP Id: rs1948231142

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72196116_72196122dup , CM000673.2:g.72196116_72196122dup	GRCh38
NC_000011.9:g.71907160_71907166dup , CM000673.1:g.71907160_71907166dup	GRCh37
NC_000011.8:g.71584808_71584814dup	NCBI36
NG_015863.1:g.11559_11565dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.713_719dup	ENSP00000308137.4:p.Ala241LeufsTer9
ENST00000393676.5:c.713_719dup MANE Select	ENSP00000377281.3:p.Ala241LeufsTer9
ENST00000675784.1:c.713_719dup	ENSP00000502440.1:p.Ala241LeufsTer9
ENST00000312293.8:c.713_719dup	ENSP00000308137.4:p.Ala241LeufsTer9
ENST00000393676.3:c.713_719dup	ENSP00000377281.3:p.Ala241LeufsTer9
ENST00000393679.5:c.713_719dup	ENSP00000377284.1:p.Ala241LeufsTer9
ENST00000393681.6:c.713_719dup	ENSP00000377286.2:p.Ala241LeufsTer9
NM_000802.3:c.713_719dup	NP_000793.1:p.Ala241LeufsTer9
NM_016724.2:c.713_719dup	NP_057936.1:p.Ala241LeufsTer9
NM_016725.2:c.713_719dup	NP_057937.1:p.Ala241LeufsTer9
NM_016729.2:c.713_719dup	NP_057941.1:p.Ala241LeufsTer9
NM_016729.3:c.713_719dup MANE Select	NP_057941.1:p.Ala241LeufsTer9
NM_016724.3:c.713_719dup	NP_057936.1:p.Ala241LeufsTer9
NM_016725.3:c.713_719dup	NP_057937.1:p.Ala241LeufsTer9