Canonical Allele Identifier: CA2202940883
Community Standard Title: NM_004380.3(CREBBP):c.4045C= (p.Gln1349=)
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740487G= , CM000678.2:g.3740487G= GRCh38
NC_000016.9:g.3790488G= , CM000678.1:g.3790488G= GRCh37
NC_000016.8:g.3730489G= NCBI36
NG_009873.1:g.144634C=
NG_009873.2:g.145227C=

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.4045C= MANE Select NP_004371.2:p.Gln1349=
ENST00000262367.10:c.4045C= MANE Select ENSP00000262367.5:p.Gln1349=
NM_001079846.1:c.3931C= NP_001073315.1:p.Gln1311=
NM_004380.2:c.4045C= NP_004371.2:p.Gln1349=
ENST00000262367.9:c.4045C= ENSP00000262367.5:p.Gln1349=
ENST00000382070.7:c.3931C= ENSP00000371502.3:p.Gln1311=
ENST00000570939.2:c.2680C= ENSP00000461002.2:p.Gln894=
ENST00000572569.1:n.509C=
ENST00000573517.6:c.351C=
ENST00000574740.1:n.127C=
ENST00000576720.1:n.2982C=
XM_005255124.3:c.4000C= XP_005255181.1:p.Gln1334=
XM_005255124.4:c.4000C= XP_005255181.1:p.Gln1334=
XM_005255125.3:c.3628C= XP_005255182.1:p.Gln1210=
XM_005255125.4:c.3628C= XP_005255182.1:p.Gln1210=
XM_006720848.2:c.4045C= XP_006720911.1:p.Gln1349=
XM_006720848.3:c.4045C= XP_006720911.1:p.Gln1349=
XM_011522380.1:c.3991C= XP_011520682.1:p.Gln1331=
XM_011522381.1:c.3292C= XP_011520683.1:p.Gln1098=
XM_011522381.2:c.3292C= XP_011520683.1:p.Gln1098=
XM_017022944.1:c.4039C= XP_016878433.1:p.Gln1347=