Canonical Allele Identifier: CA915948239

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 639442
• ClinVar RCV Id: RCV000792232
• dbSNP Id: rs1591246507

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195719_72195720delinsTG , CM000673.2:g.72195719_72195720delinsTG	GRCh38
NC_000011.9:g.71906763_71906764delinsTG , CM000673.1:g.71906763_71906764delinsTG	GRCh37
NC_000011.8:g.71584411_71584412delinsTG	NCBI36
NG_015863.1:g.11162_11163delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.465_466delinsTG	ENSP00000308137.4:p.Trp156Gly
ENST00000393676.5:c.465_466delinsTG MANE Select	ENSP00000377281.3:p.Trp156Gly
ENST00000675784.1:c.465_466delinsTG	ENSP00000502440.1:p.Trp156Gly
ENST00000312293.8:c.465_466delinsTG	ENSP00000308137.4:p.Trp156Gly
ENST00000393676.3:c.465_466delinsTG	ENSP00000377281.3:p.Trp156Gly
ENST00000393679.5:c.465_466delinsTG	ENSP00000377284.1:p.Trp156Gly
ENST00000393681.6:c.465_466delinsTG	ENSP00000377286.2:p.Trp156Gly
NM_000802.3:c.465_466delinsTG	NP_000793.1:p.Trp156Gly
NM_016724.2:c.465_466delinsTG	NP_057936.1:p.Trp156Gly
NM_016725.2:c.465_466delinsTG	NP_057937.1:p.Trp156Gly
NM_016729.2:c.465_466delinsTG	NP_057941.1:p.Trp156Gly
NM_016729.3:c.465_466delinsTG MANE Select	NP_057941.1:p.Trp156Gly
NM_016724.3:c.465_466delinsTG	NP_057936.1:p.Trp156Gly
NM_016725.3:c.465_466delinsTG	NP_057937.1:p.Trp156Gly