Canonical Allele Identifier: CA493276278

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3778063-G-T
• MyVariant Identifiers: chr16:g.3828064G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778063G>T , CM000678.2:g.3778063G>T	GRCh38
NC_000016.9:g.3828064G>T , CM000678.1:g.3828064G>T	GRCh37
NC_000016.8:g.3768065G>T	NCBI36
NG_009873.1:g.107058C>A
NG_009873.2:g.107651C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2061C>A MANE Select	ENSP00000262367.5:p.Ala687=
ENST00000262367.9:c.2061C>A	ENSP00000262367.5:p.Ala687=
ENST00000382070.7:c.1947C>A	ENSP00000371502.3:p.Ala649=
ENST00000570939.2:c.666C>A	ENSP00000461002.2:p.Ala222=
ENST00000571826.5:c.110C>A
ENST00000572134.1:c.374C>A
ENST00000634839.1:n.223C>A
NM_001079846.1:c.1947C>A	NP_001073315.1:p.Ala649=
NM_004380.2:c.2061C>A	NP_004371.2:p.Ala687=
XM_005255124.3:c.2061C>A	XP_005255181.1:p.Ala687=
XM_005255125.3:c.2061C>A	XP_005255182.1:p.Ala687=
XM_006720848.2:c.2061C>A	XP_006720911.1:p.Ala687=
XM_011522380.1:c.2007C>A	XP_011520682.1:p.Ala669=
XM_011522381.1:c.1308C>A	XP_011520683.1:p.Ala436=
XM_011522382.1:c.2061C>A	XP_011520684.1:p.Ala687=
XM_005255124.4:c.2061C>A	XP_005255181.1:p.Ala687=
XM_005255125.4:c.2061C>A	XP_005255182.1:p.Ala687=
XM_006720848.3:c.2061C>A	XP_006720911.1:p.Ala687=
XM_011522381.2:c.1308C>A	XP_011520683.1:p.Ala436=
XM_011522382.3:c.2061C>A	XP_011520684.1:p.Ala687=
XM_017022944.1:c.2061C>A	XP_016878433.1:p.Ala687=
NM_004380.3:c.2061C>A MANE Select	NP_004371.2:p.Ala687=