Canonical Allele Identifier: CA381733342

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 1354610
• ClinVar RCV Id: RCV001874173
• dbSNP Id: rs2135388722
• gnomAD v4: 11-72195673-A-T
• MyVariant Identifiers: chr11:g.71906717A>T (hg19) ; chr11:g.72195673A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195673A>T , CM000673.2:g.72195673A>T	GRCh38
NC_000011.9:g.71906717A>T , CM000673.1:g.71906717A>T	GRCh37
NC_000011.8:g.71584365A>T	NCBI36
NG_015863.1:g.11116A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.419A>T	ENSP00000308137.4:p.Glu140Val
ENST00000393676.5:c.419A>T MANE Select	ENSP00000377281.3:p.Glu140Val
ENST00000675784.1:c.419A>T	ENSP00000502440.1:p.Glu140Val
ENST00000312293.8:c.419A>T	ENSP00000308137.4:p.Glu140Val
ENST00000393676.3:c.419A>T	ENSP00000377281.3:p.Glu140Val
ENST00000393679.5:c.419A>T	ENSP00000377284.1:p.Glu140Val
ENST00000393681.6:c.419A>T	ENSP00000377286.2:p.Glu140Val
NM_000802.3:c.419A>T	NP_000793.1:p.Glu140Val
NM_016724.2:c.419A>T	NP_057936.1:p.Glu140Val
NM_016725.2:c.419A>T	NP_057937.1:p.Glu140Val
NM_016729.2:c.419A>T	NP_057941.1:p.Glu140Val
NM_016729.3:c.419A>T MANE Select	NP_057941.1:p.Glu140Val
NM_016724.3:c.419A>T	NP_057936.1:p.Glu140Val
NM_016725.3:c.419A>T	NP_057937.1:p.Glu140Val