Canonical Allele Identifier: CA394554621

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779040G>C (hg19) ; chr16:g.3729039G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729039G>C , CM000678.2:g.3729039G>C	GRCh38
NC_000016.9:g.3779040G>C , CM000678.1:g.3779040G>C	GRCh37
NC_000016.8:g.3719041G>C	NCBI36
NG_009873.1:g.156082C>G
NG_009873.2:g.156675C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6008C>G MANE Select	ENSP00000262367.5:p.Pro2003Arg
ENST00000262367.9:c.6008C>G	ENSP00000262367.5:p.Pro2003Arg
ENST00000382070.7:c.5894C>G	ENSP00000371502.3:p.Pro1965Arg
NM_001079846.1:c.5894C>G	NP_001073315.1:p.Pro1965Arg
NM_004380.2:c.6008C>G	NP_004371.2:p.Pro2003Arg
XM_005255124.3:c.5963C>G	XP_005255181.1:p.Pro1988Arg
XM_005255125.3:c.5591C>G	XP_005255182.1:p.Pro1864Arg
XM_006720848.2:c.5747C>G	XP_006720911.1:p.Pro1916Arg
XM_011522380.1:c.5954C>G	XP_011520682.1:p.Pro1985Arg
XM_011522381.1:c.5255C>G	XP_011520683.1:p.Pro1752Arg
XM_005255124.4:c.5963C>G	XP_005255181.1:p.Pro1988Arg
XM_005255125.4:c.5591C>G	XP_005255182.1:p.Pro1864Arg
XM_006720848.3:c.5747C>G	XP_006720911.1:p.Pro1916Arg
XM_011522381.2:c.5255C>G	XP_011520683.1:p.Pro1752Arg
XM_017022944.1:c.6002C>G	XP_016878433.1:p.Pro2001Arg
NM_004380.3:c.6008C>G MANE Select	NP_004371.2:p.Pro2003Arg