Canonical Allele Identifier: CA475865303
Gene: FOLR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.71906700G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195656G>T , CM000673.2:g.72195656G>T GRCh38
NC_000011.9:g.71906700G>T , CM000673.1:g.71906700G>T GRCh37
NC_000011.8:g.71584348G>T NCBI36
NG_015863.1:g.11099G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000312293.9:c.402G>T ENSP00000308137.4:p.Leu134=
ENST00000393676.5:c.402G>T MANE Select ENSP00000377281.3:p.Leu134=
ENST00000675784.1:c.402G>T ENSP00000502440.1:p.Leu134=
ENST00000312293.8:c.402G>T ENSP00000308137.4:p.Leu134=
ENST00000393676.3:c.402G>T ENSP00000377281.3:p.Leu134=
ENST00000393679.5:c.402G>T ENSP00000377284.1:p.Leu134=
ENST00000393681.6:c.402G>T ENSP00000377286.2:p.Leu134=
NM_000802.3:c.402G>T NP_000793.1:p.Leu134=
NM_016724.2:c.402G>T NP_057936.1:p.Leu134=
NM_016725.2:c.402G>T NP_057937.1:p.Leu134=
NM_016729.2:c.402G>T NP_057941.1:p.Leu134=
NM_016729.3:c.402G>T MANE Select NP_057941.1:p.Leu134=
NM_016724.3:c.402G>T NP_057936.1:p.Leu134=
NM_016725.3:c.402G>T NP_057937.1:p.Leu134=