Canonical Allele Identifier: CA394556011

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151309882
• MyVariant Identifiers: chr16:g.3779485T>G (hg19) ; chr16:g.3729484T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729484T>G , CM000678.2:g.3729484T>G	GRCh38
NC_000016.9:g.3779485T>G , CM000678.1:g.3779485T>G	GRCh37
NC_000016.8:g.3719486T>G	NCBI36
NG_009873.1:g.155637A>C
NG_009873.2:g.156230A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5563A>C MANE Select	ENSP00000262367.5:p.Ile1855Leu
ENST00000262367.9:c.5563A>C	ENSP00000262367.5:p.Ile1855Leu
ENST00000382070.7:c.5449A>C	ENSP00000371502.3:p.Ile1817Leu
NM_001079846.1:c.5449A>C	NP_001073315.1:p.Ile1817Leu
NM_004380.2:c.5563A>C	NP_004371.2:p.Ile1855Leu
XM_005255124.3:c.5518A>C	XP_005255181.1:p.Ile1840Leu
XM_005255125.3:c.5146A>C	XP_005255182.1:p.Ile1716Leu
XM_006720848.2:c.5302A>C	XP_006720911.1:p.Ile1768Leu
XM_011522380.1:c.5509A>C	XP_011520682.1:p.Ile1837Leu
XM_011522381.1:c.4810A>C	XP_011520683.1:p.Ile1604Leu
XM_005255124.4:c.5518A>C	XP_005255181.1:p.Ile1840Leu
XM_005255125.4:c.5146A>C	XP_005255182.1:p.Ile1716Leu
XM_006720848.3:c.5302A>C	XP_006720911.1:p.Ile1768Leu
XM_011522381.2:c.4810A>C	XP_011520683.1:p.Ile1604Leu
XM_017022944.1:c.5557A>C	XP_016878433.1:p.Ile1853Leu
NM_004380.3:c.5563A>C MANE Select	NP_004371.2:p.Ile1855Leu