Canonical Allele Identifier: CA394565298

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151340204
• MyVariant Identifiers: chr16:g.3790446C>G (hg19) ; chr16:g.3740445C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3740445C>G , CM000678.2:g.3740445C>G	GRCh38
NC_000016.9:g.3790446C>G , CM000678.1:g.3790446C>G	GRCh37
NC_000016.8:g.3730447C>G	NCBI36
NG_009873.1:g.144676G>C
NG_009873.2:g.145269G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.4087G>C MANE Select	ENSP00000262367.5:p.Ala1363Pro
ENST00000262367.9:c.4087G>C	ENSP00000262367.5:p.Ala1363Pro
ENST00000382070.7:c.3973G>C	ENSP00000371502.3:p.Ala1325Pro
ENST00000570939.2:c.2722G>C	ENSP00000461002.2:p.Ala908Pro
ENST00000572569.1:n.551G>C
ENST00000573517.6:c.393G>C
ENST00000574740.1:n.169G>C
ENST00000576720.1:n.3024G>C
NM_001079846.1:c.3973G>C	NP_001073315.1:p.Ala1325Pro
NM_004380.2:c.4087G>C	NP_004371.2:p.Ala1363Pro
XM_005255124.3:c.4042G>C	XP_005255181.1:p.Ala1348Pro
XM_005255125.3:c.3670G>C	XP_005255182.1:p.Ala1224Pro
XM_006720848.2:c.4087G>C	XP_006720911.1:p.Ala1363Pro
XM_011522380.1:c.4033G>C	XP_011520682.1:p.Ala1345Pro
XM_011522381.1:c.3334G>C	XP_011520683.1:p.Ala1112Pro
XM_005255124.4:c.4042G>C	XP_005255181.1:p.Ala1348Pro
XM_005255125.4:c.3670G>C	XP_005255182.1:p.Ala1224Pro
XM_006720848.3:c.4087G>C	XP_006720911.1:p.Ala1363Pro
XM_011522381.2:c.3334G>C	XP_011520683.1:p.Ala1112Pro
XM_017022944.1:c.4081G>C	XP_016878433.1:p.Ala1361Pro
NM_004380.3:c.4087G>C MANE Select	NP_004371.2:p.Ala1363Pro