Canonical Allele Identifier: CA1981879852
Gene: FOLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195191G= , CM000673.2:g.72195191G= GRCh38
NC_000011.9:g.71906235G= , CM000673.1:g.71906235G= GRCh37
NC_000011.8:g.71583883G= NCBI36
NG_015863.1:g.10634G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312293.9:c.169-80G= ENSP00000308137.4:n.169-80G=
ENST00000393676.5:c.169-80G= MANE Select ENSP00000377281.3:n.169-80G=
ENST00000675784.1:c.169-80G= ENSP00000502440.1:n.169-80G=
ENST00000312293.8:c.169-80G= ENSP00000308137.4:n.169-80G=
ENST00000393676.3:c.169-80G= ENSP00000377281.3:n.169-80G=
ENST00000393679.5:c.169-80G= ENSP00000377284.1:n.169-80G=
ENST00000393681.6:c.169-80G= ENSP00000377286.2:n.169-80G=
NM_000802.3:c.169-80G= NP_000793.1:n.169-80G=
NM_016724.2:c.169-80G= NP_057936.1:n.169-80G=
NM_016725.2:c.169-80G= NP_057937.1:n.169-80G=
NM_016729.2:c.169-80G= NP_057941.1:n.169-80G=
NM_016729.3:c.169-80G= MANE Select NP_057941.1:n.169-80G=
NM_016724.3:c.169-80G= NP_057936.1:n.169-80G=
NM_016725.3:c.169-80G= NP_057937.1:n.169-80G=