Canonical Allele Identifier: CA2792640937
Gene: FOLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72196084_72196085insC , CM000673.2:g.72196084_72196085insC GRCh38
NC_000011.9:g.71907128_71907129insC , CM000673.1:g.71907128_71907129insC GRCh37
NC_000011.8:g.71584776_71584777insC NCBI36
NG_015863.1:g.11527_11528insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000312293.9:c.681_682insC ENSP00000308137.4:p.Phe228LeufsTer20
ENST00000393676.5:c.681_682insC MANE Select ENSP00000377281.3:p.Phe228LeufsTer20
ENST00000675784.1:c.681_682insC ENSP00000502440.1:p.Phe228LeufsTer20
ENST00000312293.8:c.681_682insC ENSP00000308137.4:p.Phe228LeufsTer20
ENST00000393676.3:c.681_682insC ENSP00000377281.3:p.Phe228LeufsTer20
ENST00000393679.5:c.681_682insC ENSP00000377284.1:p.Phe228LeufsTer20
ENST00000393681.6:c.681_682insC ENSP00000377286.2:p.Phe228LeufsTer20
NM_000802.3:c.681_682insC NP_000793.1:p.Phe228LeufsTer20
NM_016724.2:c.681_682insC NP_057936.1:p.Phe228LeufsTer20
NM_016725.2:c.681_682insC NP_057937.1:p.Phe228LeufsTer20
NM_016729.2:c.681_682insC NP_057941.1:p.Phe228LeufsTer20
NM_016729.3:c.681_682insC MANE Select NP_057941.1:p.Phe228LeufsTer20
NM_016724.3:c.681_682insC NP_057936.1:p.Phe228LeufsTer20
NM_016725.3:c.681_682insC NP_057937.1:p.Phe228LeufsTer20