Canonical Allele Identifier: CA393031924
Gene: NR2E3 HGNC NCBI

Linked Data

dbSNP Id: rs1555454541
MyVariant Identifiers: chr15:g.72103796del (hg19) chr15:g.71811457del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811457del , CM000677.2:g.71811457del GRCh38
NC_000015.9:g.72103797del , CM000677.1:g.72103797del GRCh37
NC_000015.8:g.69890851del NCBI36
NG_009113.2:g.5903del

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.119-26del MANE Select ENSP00000482504.1:n.119-26del
ENST00000617575.4:c.119-26del ENSP00000482504.1:n.119-26del
ENST00000621098.1:c.119-26del ENSP00000479962.1:n.119-26del
ENST00000621736.4:c.-146-26del ENSP00000479254.1:n.-146-26del
NM_014249.3:c.119-26del NP_055064.1:n.119-26del
NM_016346.3:c.119-26del NP_057430.1:n.119-26del
XM_011521146.1:c.-146-26del XP_011519448.1:n.-146-26del
NM_014249.4:c.119-26del MANE Select NP_055064.1:n.119-26del
NM_016346.4:c.119-26del NP_057430.1:n.119-26del
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