Canonical Allele Identifier: CA493280352

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151340269
• MyVariant Identifiers: chr16:g.3790453T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3740452T>A , CM000678.2:g.3740452T>A	GRCh38
NC_000016.9:g.3790453T>A , CM000678.1:g.3790453T>A	GRCh37
NC_000016.8:g.3730454T>A	NCBI36
NG_009873.1:g.144669A>T
NG_009873.2:g.145262A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.4080A>T MANE Select	ENSP00000262367.5:p.Arg1360=
ENST00000262367.9:c.4080A>T	ENSP00000262367.5:p.Arg1360=
ENST00000382070.7:c.3966A>T	ENSP00000371502.3:p.Arg1322=
ENST00000570939.2:c.2715A>T	ENSP00000461002.2:p.Arg905=
ENST00000572569.1:n.544A>T
ENST00000573517.6:c.386A>T
ENST00000574740.1:n.162A>T
ENST00000576720.1:n.3017A>T
NM_001079846.1:c.3966A>T	NP_001073315.1:p.Arg1322=
NM_004380.2:c.4080A>T	NP_004371.2:p.Arg1360=
XM_005255124.3:c.4035A>T	XP_005255181.1:p.Arg1345=
XM_005255125.3:c.3663A>T	XP_005255182.1:p.Arg1221=
XM_006720848.2:c.4080A>T	XP_006720911.1:p.Arg1360=
XM_011522380.1:c.4026A>T	XP_011520682.1:p.Arg1342=
XM_011522381.1:c.3327A>T	XP_011520683.1:p.Arg1109=
XM_005255124.4:c.4035A>T	XP_005255181.1:p.Arg1345=
XM_005255125.4:c.3663A>T	XP_005255182.1:p.Arg1221=
XM_006720848.3:c.4080A>T	XP_006720911.1:p.Arg1360=
XM_011522381.2:c.3327A>T	XP_011520683.1:p.Arg1109=
XM_017022944.1:c.4074A>T	XP_016878433.1:p.Arg1358=
NM_004380.3:c.4080A>T MANE Select	NP_004371.2:p.Arg1360=