Canonical Allele Identifier: CA2674596793
Gene: NR2F1 HGNC NCBI

Linked Data

gnomAD v4: 5-93585399-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585401del , CM000667.2:g.93585401del GRCh38
NC_000005.9:g.92921107del , CM000667.1:g.92921107del GRCh37
NC_000005.8:g.92946863del NCBI36
NG_034119.1:g.7065del

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.303del ENSP00000481517.1:p.Asn102ThrfsTer25
ENST00000327111.8:c.378del MANE Select ENSP00000325819.3:p.Asn127ThrfsTer25
ENST00000647447.1:c.225del ENSP00000495740.1:p.Asn76ThrfsTer25
ENST00000327111.7:c.378del ENSP00000325819.3:p.Asn127ThrfsTer25
ENST00000615873.1:c.303del ENSP00000481517.1:p.Asn102ThrfsTer25
NM_005654.5:c.378del NP_005645.1:p.Asn127ThrfsTer25
NM_005654.6:c.378del MANE Select NP_005645.1:p.Asn127ThrfsTer25
Search 100 bp 5'
Search 100 bp 3'