Canonical Allele Identifier: CA2614929394
Gene: FOLR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195759_72195773dup , CM000673.2:g.72195759_72195773dup GRCh38
NC_000011.9:g.71906803_71906817dup , CM000673.1:g.71906803_71906817dup GRCh37
NC_000011.8:g.71584451_71584465dup NCBI36
NG_015863.1:g.11202_11216dup

Transcript Alleles

HGVS Amino-acid change
ENST00000312293.9:c.493+12_493+26dup ENSP00000308137.4:n.493+12_493+26dup
ENST00000393676.5:c.493+12_493+26dup MANE Select ENSP00000377281.3:n.493+12_493+26dup
ENST00000675784.1:c.493+12_493+26dup ENSP00000502440.1:n.493+12_493+26dup
ENST00000312293.8:c.493+12_493+26dup ENSP00000308137.4:n.493+12_493+26dup
ENST00000393676.3:c.493+12_493+26dup ENSP00000377281.3:n.493+12_493+26dup
ENST00000393679.5:c.493+12_493+26dup ENSP00000377284.1:n.493+12_493+26dup
ENST00000393681.6:c.493+12_493+26dup ENSP00000377286.2:n.493+12_493+26dup
NM_000802.3:c.493+12_493+26dup NP_000793.1:n.493+12_493+26dup
NM_016724.2:c.493+12_493+26dup NP_057936.1:n.493+12_493+26dup
NM_016725.2:c.493+12_493+26dup NP_057937.1:n.493+12_493+26dup
NM_016729.2:c.493+12_493+26dup NP_057941.1:n.493+12_493+26dup
NM_016729.3:c.493+12_493+26dup MANE Select NP_057941.1:n.493+12_493+26dup
NM_016724.3:c.493+12_493+26dup NP_057936.1:n.493+12_493+26dup
NM_016725.3:c.493+12_493+26dup NP_057937.1:n.493+12_493+26dup