Canonical Allele Identifier: CA1981879866

Gene: FOLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195214_72195223delinsTCTGGCTGTG , CM000673.2:g.72195214_72195223delinsTCTGGCTGTG	GRCh38
NC_000011.9:g.71906258_71906267delinsTCTGGCTGTG , CM000673.1:g.71906258_71906267delinsTCTGGCTGTG	GRCh37
NC_000011.8:g.71583906_71583915delinsTCTGGCTGTG	NCBI36
NG_015863.1:g.10657_10666delinsTCTGGCTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.169-57_169-48delinsTCTGGCTGTG	ENSP00000308137.4:n.169-57_169-48delinsTCTGGCTGTG
ENST00000393676.5:c.169-57_169-48delinsTCTGGCTGTG MANE Select	ENSP00000377281.3:n.169-57_169-48delinsTCTGGCTGTG
ENST00000675784.1:c.169-57_169-48delinsTCTGGCTGTG	ENSP00000502440.1:n.169-57_169-48delinsTCTGGCTGTG
ENST00000312293.8:c.169-57_169-48delinsTCTGGCTGTG	ENSP00000308137.4:n.169-57_169-48delinsTCTGGCTGTG
ENST00000393676.3:c.169-57_169-48delinsTCTGGCTGTG	ENSP00000377281.3:n.169-57_169-48delinsTCTGGCTGTG
ENST00000393679.5:c.169-57_169-48delinsTCTGGCTGTG	ENSP00000377284.1:n.169-57_169-48delinsTCTGGCTGTG
ENST00000393681.6:c.169-57_169-48delinsTCTGGCTGTG	ENSP00000377286.2:n.169-57_169-48delinsTCTGGCTGTG
NM_000802.3:c.169-57_169-48delinsTCTGGCTGTG	NP_000793.1:n.169-57_169-48delinsTCTGGCTGTG
NM_016724.2:c.169-57_169-48delinsTCTGGCTGTG	NP_057936.1:n.169-57_169-48delinsTCTGGCTGTG
NM_016725.2:c.169-57_169-48delinsTCTGGCTGTG	NP_057937.1:n.169-57_169-48delinsTCTGGCTGTG
NM_016729.2:c.169-57_169-48delinsTCTGGCTGTG	NP_057941.1:n.169-57_169-48delinsTCTGGCTGTG
NM_016729.3:c.169-57_169-48delinsTCTGGCTGTG MANE Select	NP_057941.1:n.169-57_169-48delinsTCTGGCTGTG
NM_016724.3:c.169-57_169-48delinsTCTGGCTGTG	NP_057936.1:n.169-57_169-48delinsTCTGGCTGTG
NM_016725.3:c.169-57_169-48delinsTCTGGCTGTG	NP_057937.1:n.169-57_169-48delinsTCTGGCTGTG