Canonical Allele Identifier: CA394555929
Community Standard Title: NM_004380.3(CREBBP):c.5600G>A (p.Arg1867Gln)
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729447C>T , CM000678.2:g.3729447C>T GRCh38
NC_000016.9:g.3779448C>T , CM000678.1:g.3779448C>T GRCh37
NC_000016.8:g.3719449C>T NCBI36
NG_009873.1:g.155674G>A
NG_009873.2:g.156267G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.5600G>A MANE Select NP_004371.2:p.Arg1867Gln
ENST00000262367.10:c.5600G>A MANE Select ENSP00000262367.5:p.Arg1867Gln
NM_001079846.1:c.5486G>A NP_001073315.1:p.Arg1829Gln
NM_004380.2:c.5600G>A NP_004371.2:p.Arg1867Gln
ENST00000262367.9:c.5600G>A ENSP00000262367.5:p.Arg1867Gln
ENST00000382070.7:c.5486G>A ENSP00000371502.3:p.Arg1829Gln
XM_005255124.3:c.5555G>A XP_005255181.1:p.Arg1852Gln
XM_005255124.4:c.5555G>A XP_005255181.1:p.Arg1852Gln
XM_005255125.3:c.5183G>A XP_005255182.1:p.Arg1728Gln
XM_005255125.4:c.5183G>A XP_005255182.1:p.Arg1728Gln
XM_006720848.2:c.5339G>A XP_006720911.1:p.Arg1780Gln
XM_006720848.3:c.5339G>A XP_006720911.1:p.Arg1780Gln
XM_011522380.1:c.5546G>A XP_011520682.1:p.Arg1849Gln
XM_011522381.1:c.4847G>A XP_011520683.1:p.Arg1616Gln
XM_011522381.2:c.4847G>A XP_011520683.1:p.Arg1616Gln
XM_017022944.1:c.5594G>A XP_016878433.1:p.Arg1865Gln