Canonical Allele Identifier: CA493279407

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151329668
• MyVariant Identifiers: chr16:g.3786738T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736737T>C , CM000678.2:g.3736737T>C	GRCh38
NC_000016.9:g.3786738T>C , CM000678.1:g.3786738T>C	GRCh37
NC_000016.8:g.3726739T>C	NCBI36
NG_009873.1:g.148384A>G
NG_009873.2:g.148977A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.4473A>G MANE Select	ENSP00000262367.5:p.Gln1491=
ENST00000262367.9:c.4473A>G	ENSP00000262367.5:p.Gln1491=
ENST00000382070.7:c.4359A>G	ENSP00000371502.3:p.Gln1453=
ENST00000570939.2:c.3108A>G	ENSP00000461002.2:p.Gln1036=
ENST00000571763.5:n.263A>G
ENST00000574740.1:n.294A>G
ENST00000576720.1:n.3296A>G
NM_001079846.1:c.4359A>G	NP_001073315.1:p.Gln1453=
NM_004380.2:c.4473A>G	NP_004371.2:p.Gln1491=
XM_005255124.3:c.4428A>G	XP_005255181.1:p.Gln1476=
XM_005255125.3:c.4056A>G	XP_005255182.1:p.Gln1352=
XM_006720848.2:c.4212A>G	XP_006720911.1:p.Gln1404=
XM_011522380.1:c.4419A>G	XP_011520682.1:p.Gln1473=
XM_011522381.1:c.3720A>G	XP_011520683.1:p.Gln1240=
XM_005255124.4:c.4428A>G	XP_005255181.1:p.Gln1476=
XM_005255125.4:c.4056A>G	XP_005255182.1:p.Gln1352=
XM_006720848.3:c.4212A>G	XP_006720911.1:p.Gln1404=
XM_011522381.2:c.3720A>G	XP_011520683.1:p.Gln1240=
XM_017022944.1:c.4467A>G	XP_016878433.1:p.Gln1489=
NM_004380.3:c.4473A>G MANE Select	NP_004371.2:p.Gln1491=