Canonical Allele Identifier: CA475865319

Gene: FOLR1

Linked Data

• MyVariant Identifiers: chr11:g.71906742C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195698C>G , CM000673.2:g.72195698C>G	GRCh38
NC_000011.9:g.71906742C>G , CM000673.1:g.71906742C>G	GRCh37
NC_000011.8:g.71584390C>G	NCBI36
NG_015863.1:g.11141C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.444C>G	ENSP00000308137.4:p.Thr148=
ENST00000393676.5:c.444C>G MANE Select	ENSP00000377281.3:p.Thr148=
ENST00000675784.1:c.444C>G	ENSP00000502440.1:p.Thr148=
ENST00000312293.8:c.444C>G	ENSP00000308137.4:p.Thr148=
ENST00000393676.3:c.444C>G	ENSP00000377281.3:p.Thr148=
ENST00000393679.5:c.444C>G	ENSP00000377284.1:p.Thr148=
ENST00000393681.6:c.444C>G	ENSP00000377286.2:p.Thr148=
NM_000802.3:c.444C>G	NP_000793.1:p.Thr148=
NM_016724.2:c.444C>G	NP_057936.1:p.Thr148=
NM_016725.2:c.444C>G	NP_057937.1:p.Thr148=
NM_016729.2:c.444C>G	NP_057941.1:p.Thr148=
NM_016729.3:c.444C>G MANE Select	NP_057941.1:p.Thr148=
NM_016724.3:c.444C>G	NP_057936.1:p.Thr148=
NM_016725.3:c.444C>G	NP_057937.1:p.Thr148=