Canonical Allele Identifier: CA8909925

Gene: RBBP8

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.22989247C>G , CM000680.2:g.22989247C>G	GRCh38
NC_000018.9:g.20569210C>G , CM000680.1:g.20569210C>G	GRCh37
NC_000018.8:g.18823208C>G	NCBI36
NG_012121.1:g.60916C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002894.3:c.736C>G MANE Select	NP_002885.1:p.Pro246Ala
ENST00000327155.10:c.736C>G MANE Select	ENSP00000323050.5:p.Pro246Ala
NM_002894.2:c.736C>G	NP_002885.1:p.Pro246Ala
NM_203291.1:c.736C>G	NP_976036.1:p.Pro246Ala
NM_203291.2:c.736C>G	NP_976036.1:p.Pro246Ala
NM_203292.1:c.736C>G	NP_976037.1:p.Pro246Ala
NM_203292.2:c.736C>G	NP_976037.1:p.Pro246Ala
ENST00000327155.9:c.736C>G	ENSP00000323050.5:p.Pro246Ala
ENST00000360790.9:c.736C>G	ENSP00000354024.5:p.Pro246Ala
ENST00000399721.6:c.736C>G	ENSP00000382627.2:p.Pro246Ala
ENST00000399722.6:c.736C>G	ENSP00000382628.2:p.Pro246Ala
ENST00000399725.6:c.736C>G	ENSP00000382630.2:p.Pro246Ala
ENST00000577445.1:c.426-25C>G
ENST00000585177.1:c.445C>G
XM_005258325.1:c.736C>G	XP_005258382.1:p.Pro246Ala
XM_005258325.3:c.736C>G	XP_005258382.1:p.Pro246Ala
XM_005258326.2:c.-87C>G	XP_005258383.1:n.-87C>G
XM_005258326.4:c.-87C>G	XP_005258383.1:n.-87C>G
XM_006722519.1:c.736C>G	XP_006722582.1:p.Pro246Ala
XM_006722519.2:c.736C>G	XP_006722582.1:p.Pro246Ala
XM_006722520.1:c.736C>G	XP_006722583.1:p.Pro246Ala
XM_006722520.2:c.736C>G	XP_006722583.1:p.Pro246Ala
XM_006722521.1:c.736C>G	XP_006722584.1:p.Pro246Ala
XM_006722521.2:c.736C>G	XP_006722584.1:p.Pro246Ala
XM_011526132.1:c.736C>G	XP_011524434.1:p.Pro246Ala
XM_011526132.2:c.736C>G	XP_011524434.1:p.Pro246Ala
XM_017025916.1:c.-87C>G	XP_016881405.1:n.-87C>G
XM_024451233.1:c.442C>G	XP_024307001.1:p.Pro148Ala