Canonical Allele Identifier: CA2289929479

Gene: RBBP8

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23022189C= , CM000680.2:g.23022189C=	GRCh38
NC_000018.9:g.20602152C= , CM000680.1:g.20602152C=	GRCh37
NC_000018.8:g.18856150C=	NCBI36
NG_012121.1:g.93858C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002894.3:c.2515C= MANE Select	NP_002885.1:p.Arg839=
ENST00000327155.10:c.2515C= MANE Select	ENSP00000323050.5:p.Arg839=
NM_002894.2:c.2515C=	NP_002885.1:p.Arg839=
NM_203291.1:c.2515C=	NP_976036.1:p.Arg839=
NM_203291.2:c.2515C=	NP_976036.1:p.Arg839=
NM_203292.1:c.2418C=	NP_976037.1:p.Thr806=
NM_203292.2:c.2418C=	NP_976037.1:p.Thr806=
ENST00000327155.9:c.2515C=	ENSP00000323050.5:p.Arg839=
ENST00000360790.9:c.2530C=	ENSP00000354024.5:p.Arg844=
ENST00000399722.6:c.2515C=	ENSP00000382628.2:p.Arg839=
ENST00000399725.6:c.2418C=	ENSP00000382630.2:p.Thr806=
ENST00000581687.1:c.49C=	ENSP00000463544.1:p.Arg17=
ENST00000583057.1:c.789C=	ENSP00000464691.1:p.Thr263=
XM_005258325.1:c.2445C=	XP_005258382.1:p.Thr815=
XM_005258325.3:c.2445C=	XP_005258382.1:p.Thr815=
XM_005258326.2:c.1693C=	XP_005258383.1:p.Arg565=
XM_005258326.4:c.1693C=	XP_005258383.1:p.Arg565=
XM_006722519.1:c.2515C=	XP_006722582.1:p.Arg839=
XM_006722519.2:c.2515C=	XP_006722582.1:p.Arg839=
XM_006722520.1:c.2515C=	XP_006722583.1:p.Arg839=
XM_006722520.2:c.2515C=	XP_006722583.1:p.Arg839=
XM_006722521.1:c.2515C=	XP_006722584.1:p.Arg839=
XM_006722521.2:c.2515C=	XP_006722584.1:p.Arg839=
XM_011526132.1:c.2515C=	XP_011524434.1:p.Arg839=
XM_011526132.2:c.2515C=	XP_011524434.1:p.Arg839=
XM_017025916.1:c.1623C=	XP_016881405.1:p.Thr541=
XM_024451233.1:c.2221C=	XP_024307001.1:p.Arg741=