Canonical Allele Identifier: CA9845329

Gene: RBL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37047071T>G , CM000682.2:g.37047071T>G	GRCh38
NC_000020.10:g.35675474T>G , CM000682.1:g.35675474T>G	GRCh37
NC_000020.9:g.35108888T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373664.8:c.1587A>C MANE Select	ENSP00000362768.3:p.Gln529His
ENST00000344359.7:c.1587A>C	ENSP00000343646.3:p.Gln529His
ENST00000373664.7:c.1587A>C	ENSP00000362768.3:p.Gln529His
NM_002895.3:c.1587A>C	NP_002886.2:p.Gln529His
NM_183404.2:c.1587A>C	NP_899662.1:p.Gln529His
XM_006723842.1:c.1071A>C	XP_006723905.1:p.Gln357His
XM_011528955.1:c.1587A>C	XP_011527257.1:p.Gln529His
XM_011528956.1:c.1350A>C	XP_011527258.1:p.Gln450His
XM_011528957.1:c.1275A>C	XP_011527259.1:p.Gln425His
XM_011528958.1:c.1587A>C	XP_011527260.1:p.Gln529His
XM_011528959.1:c.306A>C	XP_011527261.1:p.Gln102His
NM_001323281.1:c.306A>C	NP_001310210.1:p.Gln102His
NM_001323282.1:c.306A>C	NP_001310211.1:p.Gln102His
NM_002895.4:c.1587A>C	NP_002886.2:p.Gln529His
NM_183404.3:c.1587A>C	NP_899662.1:p.Gln529His
XM_006723842.3:c.1071A>C	XP_006723905.1:p.Gln357His
XM_017027992.1:c.1275A>C	XP_016883481.1:p.Gln425His
XM_024451956.1:c.1698A>C	XP_024307724.1:p.Gln566His
XM_024451957.1:c.1698A>C	XP_024307725.1:p.Gln566His
XM_024451958.1:c.1698A>C	XP_024307726.1:p.Gln566His
NM_001323281.2:c.306A>C	NP_001310210.1:p.Gln102His
NM_001323282.2:c.306A>C	NP_001310211.1:p.Gln102His
NM_002895.5:c.1587A>C MANE Select	NP_002886.2:p.Gln529His
NM_183404.4:c.1587A>C	NP_899662.1:p.Gln529His