Canonical Allele Identifier: CA1981880161
Gene: FOLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195913A= , CM000673.2:g.72195913A= GRCh38
NC_000011.9:g.71906957A= , CM000673.1:g.71906957A= GRCh37
NC_000011.8:g.71584605A= NCBI36
NG_015863.1:g.11356A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312293.9:c.510A= ENSP00000308137.4:p.Ala170=
ENST00000393676.5:c.510A= MANE Select ENSP00000377281.3:p.Ala170=
ENST00000675784.1:c.510A= ENSP00000502440.1:p.Ala170=
ENST00000312293.8:c.510A= ENSP00000308137.4:p.Ala170=
ENST00000393676.3:c.510A= ENSP00000377281.3:p.Ala170=
ENST00000393679.5:c.510A= ENSP00000377284.1:p.Ala170=
ENST00000393681.6:c.510A= ENSP00000377286.2:p.Ala170=
NM_000802.3:c.510A= NP_000793.1:p.Ala170=
NM_016724.2:c.510A= NP_057936.1:p.Ala170=
NM_016725.2:c.510A= NP_057937.1:p.Ala170=
NM_016729.2:c.510A= NP_057941.1:p.Ala170=
NM_016729.3:c.510A= MANE Select NP_057941.1:p.Ala170=
NM_016724.3:c.510A= NP_057936.1:p.Ala170=
NM_016725.3:c.510A= NP_057937.1:p.Ala170=