Canonical Allele Identifier: CA492076187
Gene: RLBP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.89755055A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211824A>T , CM000677.2:g.89211824A>T GRCh38
NC_000015.9:g.89755055A>T , CM000677.1:g.89755055A>T GRCh37
NC_000015.8:g.87556059A>T NCBI36
NG_008116.1:g.14868T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268125.10:c.603T>A MANE Select ENSP00000268125.5:p.Ile201=
ENST00000268125.9:c.603T>A ENSP00000268125.5:p.Ile201=
ENST00000563254.1:c.20T>A
ENST00000567787.1:c.*181T>A ENSP00000457251.1:n.*181T>A
NM_000326.4:c.603T>A NP_000317.1:p.Ile201=
XM_011521870.1:c.603T>A XP_011520172.1:p.Ile201=
XM_011521871.1:c.528T>A XP_011520173.1:p.Ile176=
XM_011521872.1:c.528T>A XP_011520174.1:p.Ile176=
XM_011521870.2:c.603T>A XP_011520172.1:p.Ile201=
XM_017022460.1:c.630T>A XP_016877949.1:p.Ile210=
NM_000326.5:c.603T>A MANE Select NP_000317.1:p.Ile201=