Canonical Allele Identifier: CA2614929228

Gene: FOLR1

Linked Data

• gnomAD v4: 11-72195698-C-CTCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195699_72195702dup , CM000673.2:g.72195699_72195702dup	GRCh38
NC_000011.9:g.71906743_71906746dup , CM000673.1:g.71906743_71906746dup	GRCh37
NC_000011.8:g.71584391_71584394dup	NCBI36
NG_015863.1:g.11142_11145dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.445_448dup	ENSP00000308137.4:p.Tyr150PhefsTer19
ENST00000393676.5:c.445_448dup MANE Select	ENSP00000377281.3:p.Tyr150PhefsTer19
ENST00000675784.1:c.445_448dup	ENSP00000502440.1:p.Tyr150PhefsTer19
ENST00000312293.8:c.445_448dup	ENSP00000308137.4:p.Tyr150PhefsTer19
ENST00000393676.3:c.445_448dup	ENSP00000377281.3:p.Tyr150PhefsTer19
ENST00000393679.5:c.445_448dup	ENSP00000377284.1:p.Tyr150PhefsTer19
ENST00000393681.6:c.445_448dup	ENSP00000377286.2:p.Tyr150PhefsTer19
NM_000802.3:c.445_448dup	NP_000793.1:p.Tyr150PhefsTer19
NM_016724.2:c.445_448dup	NP_057936.1:p.Tyr150PhefsTer19
NM_016725.2:c.445_448dup	NP_057937.1:p.Tyr150PhefsTer19
NM_016729.2:c.445_448dup	NP_057941.1:p.Tyr150PhefsTer19
NM_016729.3:c.445_448dup MANE Select	NP_057941.1:p.Tyr150PhefsTer19
NM_016724.3:c.445_448dup	NP_057936.1:p.Tyr150PhefsTer19
NM_016725.3:c.445_448dup	NP_057937.1:p.Tyr150PhefsTer19