Canonical Allele Identifier: CA1981880101
Gene: FOLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195765C= , CM000673.2:g.72195765C= GRCh38
NC_000011.9:g.71906809C= , CM000673.1:g.71906809C= GRCh37
NC_000011.8:g.71584457C= NCBI36
NG_015863.1:g.11208C=

Transcript Alleles

HGVS Amino-acid change
ENST00000312293.9:c.493+18C= ENSP00000308137.4:n.493+18C=
ENST00000393676.5:c.493+18C= MANE Select ENSP00000377281.3:n.493+18C=
ENST00000675784.1:c.493+18C= ENSP00000502440.1:n.493+18C=
ENST00000312293.8:c.493+18C= ENSP00000308137.4:n.493+18C=
ENST00000393676.3:c.493+18C= ENSP00000377281.3:n.493+18C=
ENST00000393679.5:c.493+18C= ENSP00000377284.1:n.493+18C=
ENST00000393681.6:c.493+18C= ENSP00000377286.2:n.493+18C=
NM_000802.3:c.493+18C= NP_000793.1:n.493+18C=
NM_016724.2:c.493+18C= NP_057936.1:n.493+18C=
NM_016725.2:c.493+18C= NP_057937.1:n.493+18C=
NM_016729.2:c.493+18C= NP_057941.1:n.493+18C=
NM_016729.3:c.493+18C= MANE Select NP_057941.1:n.493+18C=
NM_016724.3:c.493+18C= NP_057936.1:n.493+18C=
NM_016725.3:c.493+18C= NP_057937.1:n.493+18C=