Canonical Allele Identifier: CA393032479
Gene: NR2E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811802G>C , CM000677.2:g.71811802G>C GRCh38
NC_000015.9:g.72104142G>C , CM000677.1:g.72104142G>C GRCh37
NC_000015.8:g.69891196G>C NCBI36
NG_009113.2:g.6248G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.282G>C MANE Select ENSP00000482504.1:p.Lys94Asn
ENST00000617575.4:c.282G>C ENSP00000482504.1:p.Lys94Asn
ENST00000621098.1:c.282G>C ENSP00000479962.1:p.Lys94Asn
ENST00000621736.4:c.18G>C ENSP00000479254.1:p.Lys6Asn
NM_014249.3:c.282G>C NP_055064.1:p.Lys94Asn
NM_016346.3:c.282G>C NP_057430.1:p.Lys94Asn
XM_011521146.1:c.18G>C XP_011519448.1:p.Lys6Asn
NM_014249.4:c.282G>C MANE Select NP_055064.1:p.Lys94Asn
NM_016346.4:c.282G>C NP_057430.1:p.Lys94Asn