Canonical Allele Identifier: CA16618226
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs1064794459
MyVariant Identifiers: chr5:g.92929444_92929446del (hg19) chr5:g.93593738_93593740del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93593738_93593740del , CM000667.2:g.93593738_93593740del GRCh38
NC_000005.9:g.92929444_92929446del , CM000667.1:g.92929444_92929446del GRCh37
NC_000005.8:g.92955200_92955202del NCBI36
NG_034119.1:g.15402_15404del

Transcript Alleles

HGVS Amino-acid change
ENST00000502982.2:c.688_690del ENSP00000514864.1:p.Phe230del
ENST00000512697.2:c.718_720del ENSP00000514863.1:p.Phe240del
ENST00000615873.2:c.1093_1095del ENSP00000481517.1:p.Phe365del
ENST00000700211.1:c.688_690del ENSP00000514862.1:p.Phe230del
ENST00000327111.8:c.1168_1170del MANE Select ENSP00000325819.3:p.Phe390del
ENST00000647447.1:c.1015_1017del ENSP00000495740.1:p.Phe339del
ENST00000327111.7:c.1168_1170del ENSP00000325819.3:p.Phe390del
ENST00000506162.1:n.391_393del
ENST00000615873.1:c.1093_1095del ENSP00000481517.1:p.Phe365del
NM_005654.5:c.1168_1170del NP_005645.1:p.Phe390del
XM_017009797.1:c.718_720del XP_016865286.1:p.Phe240del
NM_005654.6:c.1168_1170del MANE Select NP_005645.1:p.Phe390del
Search 100 bp 5'
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