Canonical Allele Identifier: CA475865307
Gene: FOLR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.71906706A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195662A>G , CM000673.2:g.72195662A>G GRCh38
NC_000011.9:g.71906706A>G , CM000673.1:g.71906706A>G GRCh37
NC_000011.8:g.71584354A>G NCBI36
NG_015863.1:g.11105A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000312293.9:c.408A>G ENSP00000308137.4:p.Lys136=
ENST00000393676.5:c.408A>G MANE Select ENSP00000377281.3:p.Lys136=
ENST00000675784.1:c.408A>G ENSP00000502440.1:p.Lys136=
ENST00000312293.8:c.408A>G ENSP00000308137.4:p.Lys136=
ENST00000393676.3:c.408A>G ENSP00000377281.3:p.Lys136=
ENST00000393679.5:c.408A>G ENSP00000377284.1:p.Lys136=
ENST00000393681.6:c.408A>G ENSP00000377286.2:p.Lys136=
NM_000802.3:c.408A>G NP_000793.1:p.Lys136=
NM_016724.2:c.408A>G NP_057936.1:p.Lys136=
NM_016725.2:c.408A>G NP_057937.1:p.Lys136=
NM_016729.2:c.408A>G NP_057941.1:p.Lys136=
NM_016729.3:c.408A>G MANE Select NP_057941.1:p.Lys136=
NM_016724.3:c.408A>G NP_057936.1:p.Lys136=
NM_016725.3:c.408A>G NP_057937.1:p.Lys136=