Canonical Allele Identifier: CA2202937144
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3737158G= , CM000678.2:g.3737158G= GRCh38
NC_000016.9:g.3787159G= , CM000678.1:g.3787159G= GRCh37
NC_000016.8:g.3727160G= NCBI36
NG_009873.1:g.147963C=
NG_009873.2:g.148556C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4395-343C= MANE Select ENSP00000262367.5:n.4395-343C=
ENST00000262367.9:c.4395-343C= ENSP00000262367.5:n.4395-343C=
ENST00000382070.7:c.4281-343C= ENSP00000371502.3:n.4281-343C=
ENST00000570939.2:c.3030-343C= ENSP00000461002.2:n.3030-343C=
ENST00000574740.1:n.216-343C=
ENST00000576720.1:n.3218-343C=
NM_001079846.1:c.4281-343C= NP_001073315.1:n.4281-343C=
NM_004380.2:c.4395-343C= NP_004371.2:n.4395-343C=
XM_005255124.3:c.4350-343C= XP_005255181.1:n.4350-343C=
XM_005255125.3:c.3978-343C= XP_005255182.1:n.3978-343C=
XM_006720848.2:c.4134-343C= XP_006720911.1:n.4134-343C=
XM_011522380.1:c.4341-343C= XP_011520682.1:n.4341-343C=
XM_011522381.1:c.3642-343C= XP_011520683.1:n.3642-343C=
XM_005255124.4:c.4350-343C= XP_005255181.1:n.4350-343C=
XM_005255125.4:c.3978-343C= XP_005255182.1:n.3978-343C=
XM_006720848.3:c.4134-343C= XP_006720911.1:n.4134-343C=
XM_011522381.2:c.3642-343C= XP_011520683.1:n.3642-343C=
XM_017022944.1:c.4389-343C= XP_016878433.1:n.4389-343C=
NM_004380.3:c.4395-343C= MANE Select NP_004371.2:n.4395-343C=