Canonical Allele Identifier: CA1981880068

Gene: FOLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195679_72195681delinsGGT , CM000673.2:g.72195679_72195681delinsGGT	GRCh38
NC_000011.9:g.71906723_71906725delinsGGT , CM000673.1:g.71906723_71906725delinsGGT	GRCh37
NC_000011.8:g.71584371_71584373delinsGGT	NCBI36
NG_015863.1:g.11122_11124delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.425_427delinsGGT	ENSP00000308137.4:p.Trp142=
ENST00000393676.5:c.425_427delinsGGT MANE Select	ENSP00000377281.3:p.Trp142=
ENST00000675784.1:c.425_427delinsGGT	ENSP00000502440.1:p.Trp142=
ENST00000312293.8:c.425_427delinsGGT	ENSP00000308137.4:p.Trp142=
ENST00000393676.3:c.425_427delinsGGT	ENSP00000377281.3:p.Trp142=
ENST00000393679.5:c.425_427delinsGGT	ENSP00000377284.1:p.Trp142=
ENST00000393681.6:c.425_427delinsGGT	ENSP00000377286.2:p.Trp142=
NM_000802.3:c.425_427delinsGGT	NP_000793.1:p.Trp142=
NM_016724.2:c.425_427delinsGGT	NP_057936.1:p.Trp142=
NM_016725.2:c.425_427delinsGGT	NP_057937.1:p.Trp142=
NM_016729.2:c.425_427delinsGGT	NP_057941.1:p.Trp142=
NM_016729.3:c.425_427delinsGGT MANE Select	NP_057941.1:p.Trp142=
NM_016724.3:c.425_427delinsGGT	NP_057936.1:p.Trp142=
NM_016725.3:c.425_427delinsGGT	NP_057937.1:p.Trp142=