Canonical Allele Identifier: CA16607008

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 381061
• ClinVar RCV Id: RCV000434637 ; RCV001416671
• dbSNP Id: rs1057520942
• gnomAD v4: 11-72196117-C-T
• MyVariant Identifiers: chr11:g.71907161C>T (hg19) ; chr11:g.72196117C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72196117C>T , CM000673.2:g.72196117C>T	GRCh38
NC_000011.9:g.71907161C>T , CM000673.1:g.71907161C>T	GRCh37
NC_000011.8:g.71584809C>T	NCBI36
NG_015863.1:g.11560C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.714C>T	ENSP00000308137.4:p.Pro238=
ENST00000393676.5:c.714C>T MANE Select	ENSP00000377281.3:p.Pro238=
ENST00000675784.1:c.714C>T	ENSP00000502440.1:p.Pro238=
ENST00000312293.8:c.714C>T	ENSP00000308137.4:p.Pro238=
ENST00000393676.3:c.714C>T	ENSP00000377281.3:p.Pro238=
ENST00000393679.5:c.714C>T	ENSP00000377284.1:p.Pro238=
ENST00000393681.6:c.714C>T	ENSP00000377286.2:p.Pro238=
NM_000802.3:c.714C>T	NP_000793.1:p.Pro238=
NM_016724.2:c.714C>T	NP_057936.1:p.Pro238=
NM_016725.2:c.714C>T	NP_057937.1:p.Pro238=
NM_016729.2:c.714C>T	NP_057941.1:p.Pro238=
NM_016729.3:c.714C>T MANE Select	NP_057941.1:p.Pro238=
NM_016724.3:c.714C>T	NP_057936.1:p.Pro238=
NM_016725.3:c.714C>T	NP_057937.1:p.Pro238=