Canonical Allele Identifier: CA2574912493

Gene: FOLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72196188C>G , CM000673.2:g.72196188C>G	GRCh38
NC_000011.9:g.71907232C>G , CM000673.1:g.71907232C>G	GRCh37
NC_000011.8:g.71584880C>G	NCBI36
NG_015863.1:g.11631C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.*11C>G	ENSP00000308137.4:n.*11C>G
ENST00000393676.5:c.*11C>G MANE Select	ENSP00000377281.3:n.*11C>G
ENST00000675784.1:c.*11C>G	ENSP00000502440.1:n.*11C>G
ENST00000312293.8:c.*11C>G	ENSP00000308137.4:n.*11C>G
ENST00000393676.3:c.*11C>G	ENSP00000377281.3:n.*11C>G
ENST00000393679.5:c.*11C>G	ENSP00000377284.1:n.*11C>G
ENST00000393681.6:c.*11C>G	ENSP00000377286.2:n.*11C>G
NM_000802.3:c.*11C>G	NP_000793.1:n.*11C>G
NM_016724.2:c.*11C>G	NP_057936.1:n.*11C>G
NM_016725.2:c.*11C>G	NP_057937.1:n.*11C>G
NM_016729.2:c.*11C>G	NP_057941.1:n.*11C>G
NM_016729.3:c.*11C>G MANE Select	NP_057941.1:n.*11C>G
NM_016724.3:c.*11C>G	NP_057936.1:n.*11C>G
NM_016725.3:c.*11C>G	NP_057937.1:n.*11C>G