Canonical Allele Identifier: CA8910175

Gene: RBBP8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.22993867del , CM000680.2:g.22993867del	GRCh38
NC_000018.9:g.20573830del , CM000680.1:g.20573830del	GRCh37
NC_000018.8:g.18827828del	NCBI36
NG_012121.1:g.65536del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327155.10:c.1939+20del MANE Select	ENSP00000323050.5:n.1939+20del
ENST00000327155.9:c.1939+20del	ENSP00000323050.5:n.1939+20del
ENST00000360790.9:c.1939+20del	ENSP00000354024.5:n.1939+20del
ENST00000399722.6:c.1939+20del	ENSP00000382628.2:n.1939+20del
ENST00000399725.6:c.1939+20del	ENSP00000382630.2:n.1939+20del
ENST00000583057.1:c.283+20del	ENSP00000464691.1:n.283+20del
NM_002894.2:c.1939+20del	NP_002885.1:n.1939+20del
NM_203291.1:c.1939+20del	NP_976036.1:n.1939+20del
NM_203292.1:c.1939+20del	NP_976037.1:n.1939+20del
XM_005258325.1:c.1939+20del	XP_005258382.1:n.1939+20del
XM_005258326.2:c.1117+20del	XP_005258383.1:n.1117+20del
XM_006722519.1:c.1939+20del	XP_006722582.1:n.1939+20del
XM_006722520.1:c.1939+20del	XP_006722583.1:n.1939+20del
XM_006722521.1:c.1939+20del	XP_006722584.1:n.1939+20del
XM_011526132.1:c.1939+20del	XP_011524434.1:n.1939+20del
XM_005258325.3:c.1939+20del	XP_005258382.1:n.1939+20del
XM_005258326.4:c.1117+20del	XP_005258383.1:n.1117+20del
XM_006722519.2:c.1939+20del	XP_006722582.1:n.1939+20del
XM_006722520.2:c.1939+20del	XP_006722583.1:n.1939+20del
XM_006722521.2:c.1939+20del	XP_006722584.1:n.1939+20del
XM_011526132.2:c.1939+20del	XP_011524434.1:n.1939+20del
XM_017025916.1:c.1117+20del	XP_016881405.1:n.1117+20del
XM_024451233.1:c.1645+20del	XP_024307001.1:n.1645+20del
NM_002894.3:c.1939+20del MANE Select	NP_002885.1:n.1939+20del
NM_203291.2:c.1939+20del	NP_976036.1:n.1939+20del
NM_203292.2:c.1939+20del	NP_976037.1:n.1939+20del