Canonical Allele Identifier: CA394553771
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728783G>T , CM000678.2:g.3728783G>T GRCh38
NC_000016.9:g.3778784G>T , CM000678.1:g.3778784G>T GRCh37
NC_000016.8:g.3718785G>T NCBI36
NG_009873.1:g.156338C>A
NG_009873.2:g.156931C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6264C>A MANE Select ENSP00000262367.5:p.Asn2088Lys
ENST00000262367.9:c.6264C>A ENSP00000262367.5:p.Asn2088Lys
ENST00000382070.7:c.6150C>A ENSP00000371502.3:p.Asn2050Lys
NM_001079846.1:c.6150C>A NP_001073315.1:p.Asn2050Lys
NM_004380.2:c.6264C>A NP_004371.2:p.Asn2088Lys
XM_005255124.3:c.6219C>A XP_005255181.1:p.Asn2073Lys
XM_005255125.3:c.5847C>A XP_005255182.1:p.Asn1949Lys
XM_006720848.2:c.6003C>A XP_006720911.1:p.Asn2001Lys
XM_011522380.1:c.6210C>A XP_011520682.1:p.Asn2070Lys
XM_011522381.1:c.5511C>A XP_011520683.1:p.Asn1837Lys
XM_005255124.4:c.6219C>A XP_005255181.1:p.Asn2073Lys
XM_005255125.4:c.5847C>A XP_005255182.1:p.Asn1949Lys
XM_006720848.3:c.6003C>A XP_006720911.1:p.Asn2001Lys
XM_011522381.2:c.5511C>A XP_011520683.1:p.Asn1837Lys
XM_017022944.1:c.6258C>A XP_016878433.1:p.Asn2086Lys
NM_004380.3:c.6264C>A MANE Select NP_004371.2:p.Asn2088Lys