Canonical Allele Identifier: CA2194510020
Gene: RLBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211687_89211689delinsCCT , CM000677.2:g.89211687_89211689delinsCCT GRCh38
NC_000015.9:g.89754918_89754920delinsCCT , CM000677.1:g.89754918_89754920delinsCCT GRCh37
NC_000015.8:g.87555922_87555924delinsCCT NCBI36
NG_008116.1:g.15003_15005delinsAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000268125.10:c.684+54_684+56delinsAGG MANE Select ENSP00000268125.5:n.684+54_684+56delinsAGG
ENST00000268125.9:c.684+54_684+56delinsAGG ENSP00000268125.5:n.684+54_684+56delinsAGG
ENST00000563254.1:c.101+54_101+56delinsAGG
ENST00000567787.1:c.*262+54_*262+56delinsAGG ENSP00000457251.1:n.*262+54_*262+56delinsAGG
NM_000326.4:c.684+54_684+56delinsAGG NP_000317.1:n.684+54_684+56delinsAGG
XM_011521870.1:c.684+54_684+56delinsAGG XP_011520172.1:n.684+54_684+56delinsAGG
XM_011521871.1:c.609+54_609+56delinsAGG XP_011520173.1:n.609+54_609+56delinsAGG
XM_011521872.1:c.609+54_609+56delinsAGG XP_011520174.1:n.609+54_609+56delinsAGG
XM_011521870.2:c.684+54_684+56delinsAGG XP_011520172.1:n.684+54_684+56delinsAGG
XM_017022460.1:c.711+54_711+56delinsAGG XP_016877949.1:n.711+54_711+56delinsAGG
NM_000326.5:c.684+54_684+56delinsAGG MANE Select NP_000317.1:n.684+54_684+56delinsAGG