Canonical Allele Identifier: CA2202940832
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740451C= , CM000678.2:g.3740451C= GRCh38
NC_000016.9:g.3790452C= , CM000678.1:g.3790452C= GRCh37
NC_000016.8:g.3730453C= NCBI36
NG_009873.1:g.144670G=
NG_009873.2:g.145263G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4081G= MANE Select ENSP00000262367.5:p.Val1361=
ENST00000262367.9:c.4081G= ENSP00000262367.5:p.Val1361=
ENST00000382070.7:c.3967G= ENSP00000371502.3:p.Val1323=
ENST00000570939.2:c.2716G= ENSP00000461002.2:p.Val906=
ENST00000572569.1:n.545G=
ENST00000573517.6:c.387G=
ENST00000574740.1:n.163G=
ENST00000576720.1:n.3018G=
NM_001079846.1:c.3967G= NP_001073315.1:p.Val1323=
NM_004380.2:c.4081G= NP_004371.2:p.Val1361=
XM_005255124.3:c.4036G= XP_005255181.1:p.Val1346=
XM_005255125.3:c.3664G= XP_005255182.1:p.Val1222=
XM_006720848.2:c.4081G= XP_006720911.1:p.Val1361=
XM_011522380.1:c.4027G= XP_011520682.1:p.Val1343=
XM_011522381.1:c.3328G= XP_011520683.1:p.Val1110=
XM_005255124.4:c.4036G= XP_005255181.1:p.Val1346=
XM_005255125.4:c.3664G= XP_005255182.1:p.Val1222=
XM_006720848.3:c.4081G= XP_006720911.1:p.Val1361=
XM_011522381.2:c.3328G= XP_011520683.1:p.Val1110=
XM_017022944.1:c.4075G= XP_016878433.1:p.Val1359=
NM_004380.3:c.4081G= MANE Select NP_004371.2:p.Val1361=