Canonical Allele Identifier: CA394556073

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310088
• MyVariant Identifiers: chr16:g.3779512T>A (hg19) ; chr16:g.3729511T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729511T>A , CM000678.2:g.3729511T>A	GRCh38
NC_000016.9:g.3779512T>A , CM000678.1:g.3779512T>A	GRCh37
NC_000016.8:g.3719513T>A	NCBI36
NG_009873.1:g.155610A>T
NG_009873.2:g.156203A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5536A>T MANE Select	ENSP00000262367.5:p.Ile1846Phe
ENST00000262367.9:c.5536A>T	ENSP00000262367.5:p.Ile1846Phe
ENST00000382070.7:c.5422A>T	ENSP00000371502.3:p.Ile1808Phe
NM_001079846.1:c.5422A>T	NP_001073315.1:p.Ile1808Phe
NM_004380.2:c.5536A>T	NP_004371.2:p.Ile1846Phe
XM_005255124.3:c.5491A>T	XP_005255181.1:p.Ile1831Phe
XM_005255125.3:c.5119A>T	XP_005255182.1:p.Ile1707Phe
XM_006720848.2:c.5275A>T	XP_006720911.1:p.Ile1759Phe
XM_011522380.1:c.5482A>T	XP_011520682.1:p.Ile1828Phe
XM_011522381.1:c.4783A>T	XP_011520683.1:p.Ile1595Phe
XM_005255124.4:c.5491A>T	XP_005255181.1:p.Ile1831Phe
XM_005255125.4:c.5119A>T	XP_005255182.1:p.Ile1707Phe
XM_006720848.3:c.5275A>T	XP_006720911.1:p.Ile1759Phe
XM_011522381.2:c.4783A>T	XP_011520683.1:p.Ile1595Phe
XM_017022944.1:c.5530A>T	XP_016878433.1:p.Ile1844Phe
NM_004380.3:c.5536A>T MANE Select	NP_004371.2:p.Ile1846Phe