Canonical Allele Identifier: CA1139662085

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 975231
• ClinVar RCV Id: RCV001251756
• dbSNP Id: rs1948222554

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195754G>T , CM000673.2:g.72195754G>T	GRCh38
NC_000011.9:g.71906798G>T , CM000673.1:g.71906798G>T	GRCh37
NC_000011.8:g.71584446G>T	NCBI36
NG_015863.1:g.11197G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000312293.9:c.493+7G>T	ENSP00000308137.4:n.493+7G>T
ENST00000393676.5:c.493+7G>T MANE Select	ENSP00000377281.3:n.493+7G>T
ENST00000675784.1:c.493+7G>T	ENSP00000502440.1:n.493+7G>T
ENST00000312293.8:c.493+7G>T	ENSP00000308137.4:n.493+7G>T
ENST00000393676.3:c.493+7G>T	ENSP00000377281.3:n.493+7G>T
ENST00000393679.5:c.493+7G>T	ENSP00000377284.1:n.493+7G>T
ENST00000393681.6:c.493+7G>T	ENSP00000377286.2:n.493+7G>T
NM_000802.3:c.493+7G>T	NP_000793.1:n.493+7G>T
NM_016724.2:c.493+7G>T	NP_057936.1:n.493+7G>T
NM_016725.2:c.493+7G>T	NP_057937.1:n.493+7G>T
NM_016729.2:c.493+7G>T	NP_057941.1:n.493+7G>T
NM_016729.3:c.493+7G>T MANE Select	NP_057941.1:n.493+7G>T
NM_016724.3:c.493+7G>T	NP_057936.1:n.493+7G>T
NM_016725.3:c.493+7G>T	NP_057937.1:n.493+7G>T