Canonical Allele Identifier: CA16606020

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 382335
• ClinVar RCV Id: RCV000426509
• dbSNP Id: rs1057521333
• gnomAD v2: 11-71906638-T-A
• gnomAD v4: 11-72195594-T-A
• MyVariant Identifiers: chr11:g.71906638T>A (hg19) ; chr11:g.72195594T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195594T>A , CM000673.2:g.72195594T>A	GRCh38
NC_000011.9:g.71906638T>A , CM000673.1:g.71906638T>A	GRCh37
NC_000011.8:g.71584286T>A	NCBI36
NG_015863.1:g.11037T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.358-18T>A	ENSP00000308137.4:n.358-18T>A
ENST00000393676.5:c.358-18T>A MANE Select	ENSP00000377281.3:n.358-18T>A
ENST00000675784.1:c.358-18T>A	ENSP00000502440.1:n.358-18T>A
ENST00000312293.8:c.358-18T>A	ENSP00000308137.4:n.358-18T>A
ENST00000393676.3:c.358-18T>A	ENSP00000377281.3:n.358-18T>A
ENST00000393679.5:c.358-18T>A	ENSP00000377284.1:n.358-18T>A
ENST00000393681.6:c.358-18T>A	ENSP00000377286.2:n.358-18T>A
NM_000802.3:c.358-18T>A	NP_000793.1:n.358-18T>A
NM_016724.2:c.358-18T>A	NP_057936.1:n.358-18T>A
NM_016725.2:c.358-18T>A	NP_057937.1:n.358-18T>A
NM_016729.2:c.358-18T>A	NP_057941.1:n.358-18T>A
NM_016729.3:c.358-18T>A MANE Select	NP_057941.1:n.358-18T>A
NM_016724.3:c.358-18T>A	NP_057936.1:n.358-18T>A
NM_016725.3:c.358-18T>A	NP_057937.1:n.358-18T>A