Canonical Allele Identifier: CA6169148
Gene: FOLR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2009251
ClinVar RCV Id: RCV002838227
dbSNP Id: rs775864895

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195393A>T , CM000673.2:g.72195393A>T GRCh38
NC_000011.9:g.71906437A>T , CM000673.1:g.71906437A>T GRCh37
NC_000011.8:g.71584085A>T NCBI36
NG_015863.1:g.10836A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000312293.9:c.291A>T ENSP00000308137.4:p.Lys97Asn
ENST00000393676.5:c.291A>T MANE Select ENSP00000377281.3:p.Lys97Asn
ENST00000675784.1:c.291A>T ENSP00000502440.1:p.Lys97Asn
ENST00000312293.8:c.291A>T ENSP00000308137.4:p.Lys97Asn
ENST00000393676.3:c.291A>T ENSP00000377281.3:p.Lys97Asn
ENST00000393679.5:c.291A>T ENSP00000377284.1:p.Lys97Asn
ENST00000393681.6:c.291A>T ENSP00000377286.2:p.Lys97Asn
NM_000802.3:c.291A>T NP_000793.1:p.Lys97Asn
NM_016724.2:c.291A>T NP_057936.1:p.Lys97Asn
NM_016725.2:c.291A>T NP_057937.1:p.Lys97Asn
NM_016729.2:c.291A>T NP_057941.1:p.Lys97Asn
NM_016729.3:c.291A>T MANE Select NP_057941.1:p.Lys97Asn
NM_016724.3:c.291A>T NP_057936.1:p.Lys97Asn
NM_016725.3:c.291A>T NP_057937.1:p.Lys97Asn