Canonical Allele Identifier: CA394562494
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2141285295
gnomAD v4: 16-3793434-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3793434T>A , CM000678.2:g.3793434T>A GRCh38
NC_000016.9:g.3843435T>A , CM000678.1:g.3843435T>A GRCh37
NC_000016.8:g.3783436T>A NCBI36
NG_009873.1:g.91687A>T
NG_009873.2:g.92280A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.1168A>T MANE Select ENSP00000262367.5:p.Asn390Tyr
ENST00000262367.9:c.1168A>T ENSP00000262367.5:p.Asn390Tyr
ENST00000382070.7:c.1168A>T ENSP00000371502.3:p.Asn390Tyr
NM_001079846.1:c.1168A>T NP_001073315.1:p.Asn390Tyr
NM_004380.2:c.1168A>T NP_004371.2:p.Asn390Tyr
XM_005255124.3:c.1168A>T XP_005255181.1:p.Asn390Tyr
XM_005255125.3:c.1168A>T XP_005255182.1:p.Asn390Tyr
XM_006720848.2:c.1168A>T XP_006720911.1:p.Asn390Tyr
XM_011522380.1:c.1114A>T XP_011520682.1:p.Asn372Tyr
XM_011522381.1:c.415A>T XP_011520683.1:p.Asn139Tyr
XM_011522382.1:c.1168A>T XP_011520684.1:p.Asn390Tyr
XM_005255124.4:c.1168A>T XP_005255181.1:p.Asn390Tyr
XM_005255125.4:c.1168A>T XP_005255182.1:p.Asn390Tyr
XM_006720848.3:c.1168A>T XP_006720911.1:p.Asn390Tyr
XM_011522381.2:c.415A>T XP_011520683.1:p.Asn139Tyr
XM_011522382.3:c.1168A>T XP_011520684.1:p.Asn390Tyr
XM_017022944.1:c.1168A>T XP_016878433.1:p.Asn390Tyr
NM_004380.3:c.1168A>T MANE Select NP_004371.2:p.Asn390Tyr