Canonical Allele Identifier: CA2538702629
Gene: FOLR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72196203_72196210del , CM000673.2:g.72196203_72196210del GRCh38
NC_000011.9:g.71907247_71907254del , CM000673.1:g.71907247_71907254del GRCh37
NC_000011.8:g.71584895_71584902del NCBI36
NG_015863.1:g.11646_11653del

Transcript Alleles

HGVS Amino-acid Change
ENST00000312293.9:c.*26_*33del ENSP00000308137.4:n.*26_*33del
ENST00000393676.5:c.*26_*33del MANE Select ENSP00000377281.3:n.*26_*33del
ENST00000675784.1:c.*26_*33del ENSP00000502440.1:n.*26_*33del
ENST00000312293.8:c.*26_*33del ENSP00000308137.4:n.*26_*33del
ENST00000393676.3:c.*26_*33del ENSP00000377281.3:n.*26_*33del
ENST00000393679.5:c.*26_*33del ENSP00000377284.1:n.*26_*33del
ENST00000393681.6:c.*26_*33del ENSP00000377286.2:n.*26_*33del
NM_000802.3:c.*26_*33del NP_000793.1:n.*26_*33del
NM_016724.2:c.*26_*33del NP_057936.1:n.*26_*33del
NM_016725.2:c.*26_*33del NP_057937.1:n.*26_*33del
NM_016729.2:c.*26_*33del NP_057941.1:n.*26_*33del
NM_016729.3:c.*26_*33del MANE Select NP_057941.1:n.*26_*33del
NM_016724.3:c.*26_*33del NP_057936.1:n.*26_*33del
NM_016725.3:c.*26_*33del NP_057937.1:n.*26_*33del