Canonical Allele Identifier: CA210020
Community Standard Title: NM_000326.5(RLBP1):c.286_297del (p.Phe96_Phe99del)
Gene: RLBP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89217174_89217185del , CM000677.2:g.89217174_89217185del GRCh38
NC_000015.9:g.89760405_89760416del , CM000677.1:g.89760405_89760416del GRCh37
NC_000015.8:g.87561409_87561420del NCBI36
NG_008116.1:g.9512_9523del

Transcript Alleles

HGVS Amino-acid Change
NM_000326.5:c.286_297del MANE Select NP_000317.1:p.Phe96_Phe99del
ENST00000268125.10:c.286_297del MANE Select ENSP00000268125.5:p.Phe96_Phe99del
NM_000326.4:c.286_297del NP_000317.1:p.Phe96_Phe99del
ENST00000268125.9:c.286_297del ENSP00000268125.5:p.Phe96_Phe99del
ENST00000567787.1:c.183+103_183+114del ENSP00000457251.1:n.183+103_183+114del
XM_011521870.1:c.286_297del XP_011520172.1:p.Phe96_Phe99del
XM_011521870.2:c.286_297del XP_011520172.1:p.Phe96_Phe99del
XM_011521871.1:c.211_222del XP_011520173.1:p.Phe71_Phe74del
XM_011521872.1:c.211_222del XP_011520174.1:p.Phe71_Phe74del
XM_017022460.1:c.313_324del XP_016877949.1:p.Phe105_Phe108del
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