Canonical Allele Identifier: CA2499221294

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 1042653
• ClinVar RCV Id: RCV001346644

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72196050_72196051delinsTG , CM000673.2:g.72196050_72196051delinsTG	GRCh38
NC_000011.9:g.71907094_71907095delinsTG , CM000673.1:g.71907094_71907095delinsTG	GRCh37
NC_000011.8:g.71584742_71584743delinsTG	NCBI36
NG_015863.1:g.11493_11494delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.647_648delinsTG	ENSP00000308137.4:p.Pro216Leu
ENST00000393676.5:c.647_648delinsTG MANE Select	ENSP00000377281.3:p.Pro216Leu
ENST00000675784.1:c.647_648delinsTG	ENSP00000502440.1:p.Pro216Leu
ENST00000312293.8:c.647_648delinsTG	ENSP00000308137.4:p.Pro216Leu
ENST00000393676.3:c.647_648delinsTG	ENSP00000377281.3:p.Pro216Leu
ENST00000393679.5:c.647_648delinsTG	ENSP00000377284.1:p.Pro216Leu
ENST00000393681.6:c.647_648delinsTG	ENSP00000377286.2:p.Pro216Leu
NM_000802.3:c.647_648delinsTG	NP_000793.1:p.Pro216Leu
NM_016724.2:c.647_648delinsTG	NP_057936.1:p.Pro216Leu
NM_016725.2:c.647_648delinsTG	NP_057937.1:p.Pro216Leu
NM_016729.2:c.647_648delinsTG	NP_057941.1:p.Pro216Leu
NM_016729.3:c.647_648delinsTG MANE Select	NP_057941.1:p.Pro216Leu
NM_016724.3:c.647_648delinsTG	NP_057936.1:p.Pro216Leu
NM_016725.3:c.647_648delinsTG	NP_057937.1:p.Pro216Leu