Canonical Allele Identifier: CA1981879851

Gene: FOLR1

Linked Data

• dbSNP Id: rs1948210088
• gnomAD v4: 11-72195189-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195193del , CM000673.2:g.72195193del	GRCh38
NC_000011.9:g.71906237del , CM000673.1:g.71906237del	GRCh37
NC_000011.8:g.71583885del	NCBI36
NG_015863.1:g.10636del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.169-78del	ENSP00000308137.4:n.169-78del
ENST00000393676.5:c.169-78del MANE Select	ENSP00000377281.3:n.169-78del
ENST00000675784.1:c.169-78del	ENSP00000502440.1:n.169-78del
ENST00000312293.8:c.169-78del	ENSP00000308137.4:n.169-78del
ENST00000393676.3:c.169-78del	ENSP00000377281.3:n.169-78del
ENST00000393679.5:c.169-78del	ENSP00000377284.1:n.169-78del
ENST00000393681.6:c.169-78del	ENSP00000377286.2:n.169-78del
NM_000802.3:c.169-78del	NP_000793.1:n.169-78del
NM_016724.2:c.169-78del	NP_057936.1:n.169-78del
NM_016725.2:c.169-78del	NP_057937.1:n.169-78del
NM_016729.2:c.169-78del	NP_057941.1:n.169-78del
NM_016729.3:c.169-78del MANE Select	NP_057941.1:n.169-78del
NM_016724.3:c.169-78del	NP_057936.1:n.169-78del
NM_016725.3:c.169-78del	NP_057937.1:n.169-78del