Canonical Allele Identifier: CA394563283

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3786658T>C (hg19) ; chr16:g.3736657T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736657T>C , CM000678.2:g.3736657T>C	GRCh38
NC_000016.9:g.3786658T>C , CM000678.1:g.3786658T>C	GRCh37
NC_000016.8:g.3726659T>C	NCBI36
NG_009873.1:g.148464A>G
NG_009873.2:g.149057A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4553A>G MANE Select	ENSP00000262367.5:p.Asp1518Gly
ENST00000262367.9:c.4553A>G	ENSP00000262367.5:p.Asp1518Gly
ENST00000382070.7:c.4439A>G	ENSP00000371502.3:p.Asp1480Gly
ENST00000570939.2:c.3188A>G	ENSP00000461002.2:p.Asp1063Gly
ENST00000571763.5:n.343A>G
ENST00000574740.1:n.374A>G
ENST00000576720.1:n.3376A>G
NM_001079846.1:c.4439A>G	NP_001073315.1:p.Asp1480Gly
NM_004380.2:c.4553A>G	NP_004371.2:p.Asp1518Gly
XM_005255124.3:c.4508A>G	XP_005255181.1:p.Asp1503Gly
XM_005255125.3:c.4136A>G	XP_005255182.1:p.Asp1379Gly
XM_006720848.2:c.4292A>G	XP_006720911.1:p.Asp1431Gly
XM_011522380.1:c.4499A>G	XP_011520682.1:p.Asp1500Gly
XM_011522381.1:c.3800A>G	XP_011520683.1:p.Asp1267Gly
XM_005255124.4:c.4508A>G	XP_005255181.1:p.Asp1503Gly
XM_005255125.4:c.4136A>G	XP_005255182.1:p.Asp1379Gly
XM_006720848.3:c.4292A>G	XP_006720911.1:p.Asp1431Gly
XM_011522381.2:c.3800A>G	XP_011520683.1:p.Asp1267Gly
XM_017022944.1:c.4547A>G	XP_016878433.1:p.Asp1516Gly
NM_004380.3:c.4553A>G MANE Select	NP_004371.2:p.Asp1518Gly