Canonical Allele Identifier: CA493393059

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3777752C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727751C>G , CM000678.2:g.3727751C>G	GRCh38
NC_000016.9:g.3777752C>G , CM000678.1:g.3777752C>G	GRCh37
NC_000016.8:g.3717753C>G	NCBI36
NG_009873.1:g.157370G>C
NG_009873.2:g.157963G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7296G>C MANE Select	ENSP00000262367.5:p.Gly2432=
ENST00000262367.9:c.7296G>C	ENSP00000262367.5:p.Gly2432=
ENST00000382070.7:c.7182G>C	ENSP00000371502.3:p.Gly2394=
NM_001079846.1:c.7182G>C	NP_001073315.1:p.Gly2394=
NM_004380.2:c.7296G>C	NP_004371.2:p.Gly2432=
XM_005255124.3:c.7251G>C	XP_005255181.1:p.Gly2417=
XM_005255125.3:c.6879G>C	XP_005255182.1:p.Gly2293=
XM_006720848.2:c.7035G>C	XP_006720911.1:p.Gly2345=
XM_011522380.1:c.7242G>C	XP_011520682.1:p.Gly2414=
XM_011522381.1:c.6543G>C	XP_011520683.1:p.Gly2181=
XM_005255124.4:c.7251G>C	XP_005255181.1:p.Gly2417=
XM_005255125.4:c.6879G>C	XP_005255182.1:p.Gly2293=
XM_006720848.3:c.7035G>C	XP_006720911.1:p.Gly2345=
XM_011522381.2:c.6543G>C	XP_011520683.1:p.Gly2181=
XM_017022944.1:c.7290G>C	XP_016878433.1:p.Gly2430=
NM_004380.3:c.7296G>C MANE Select	NP_004371.2:p.Gly2432=