Canonical Allele Identifier: CA7722278
Community Standard Title: NM_000326.5(RLBP1):c.466C>T (p.Arg156Ter)
Gene: RLBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89215119G>A , CM000677.2:g.89215119G>A GRCh38
NC_000015.9:g.89758350G>A , CM000677.1:g.89758350G>A GRCh37
NC_000015.8:g.87559354G>A NCBI36
NG_008116.1:g.11573C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000326.5:c.466C>T MANE Select NP_000317.1:p.Arg156Ter
ENST00000268125.10:c.466C>T MANE Select ENSP00000268125.5:p.Arg156Ter
NM_000326.4:c.466C>T NP_000317.1:p.Arg156Ter
ENST00000268125.9:c.466C>T ENSP00000268125.5:p.Arg156Ter
ENST00000567787.1:c.*44C>T ENSP00000457251.1:n.*44C>T
XM_011521870.1:c.466C>T XP_011520172.1:p.Arg156Ter
XM_011521870.2:c.466C>T XP_011520172.1:p.Arg156Ter
XM_011521871.1:c.391C>T XP_011520173.1:p.Arg131Ter
XM_011521872.1:c.391C>T XP_011520174.1:p.Arg131Ter
XM_017022460.1:c.493C>T XP_016877949.1:p.Arg165Ter