Canonical Allele Identifier: CA493276258

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3828037T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778036T>G , CM000678.2:g.3778036T>G	GRCh38
NC_000016.9:g.3828037T>G , CM000678.1:g.3828037T>G	GRCh37
NC_000016.8:g.3768038T>G	NCBI36
NG_009873.1:g.107085A>C
NG_009873.2:g.107678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2088A>C MANE Select	ENSP00000262367.5:p.Pro696=
ENST00000262367.9:c.2088A>C	ENSP00000262367.5:p.Pro696=
ENST00000382070.7:c.1974A>C	ENSP00000371502.3:p.Pro658=
ENST00000570939.2:c.693A>C	ENSP00000461002.2:p.Pro231=
ENST00000571826.5:c.137A>C
ENST00000572134.1:c.401A>C
ENST00000634839.1:n.250A>C
NM_001079846.1:c.1974A>C	NP_001073315.1:p.Pro658=
NM_004380.2:c.2088A>C	NP_004371.2:p.Pro696=
XM_005255124.3:c.2088A>C	XP_005255181.1:p.Pro696=
XM_005255125.3:c.2088A>C	XP_005255182.1:p.Pro696=
XM_006720848.2:c.2088A>C	XP_006720911.1:p.Pro696=
XM_011522380.1:c.2034A>C	XP_011520682.1:p.Pro678=
XM_011522381.1:c.1335A>C	XP_011520683.1:p.Pro445=
XM_011522382.1:c.2088A>C	XP_011520684.1:p.Pro696=
XM_005255124.4:c.2088A>C	XP_005255181.1:p.Pro696=
XM_005255125.4:c.2088A>C	XP_005255182.1:p.Pro696=
XM_006720848.3:c.2088A>C	XP_006720911.1:p.Pro696=
XM_011522381.2:c.1335A>C	XP_011520683.1:p.Pro445=
XM_011522382.3:c.2088A>C	XP_011520684.1:p.Pro696=
XM_017022944.1:c.2088A>C	XP_016878433.1:p.Pro696=
NM_004380.3:c.2088A>C MANE Select	NP_004371.2:p.Pro696=