Canonical Allele Identifier: CA394557642

Gene: CREBBP

Linked Data

• dbSNP Id: rs772591687
• gnomAD v4: 16-3729831-G-T
• MyVariant Identifiers: chr16:g.3779832G>T (hg19) ; chr16:g.3729831G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729831G>T , CM000678.2:g.3729831G>T	GRCh38
NC_000016.9:g.3779832G>T , CM000678.1:g.3779832G>T	GRCh37
NC_000016.8:g.3719833G>T	NCBI36
NG_009873.1:g.155290C>A
NG_009873.2:g.155883C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5216C>A MANE Select	ENSP00000262367.5:p.Ala1739Asp
ENST00000262367.9:c.5216C>A	ENSP00000262367.5:p.Ala1739Asp
ENST00000382070.7:c.5102C>A	ENSP00000371502.3:p.Ala1701Asp
NM_001079846.1:c.5102C>A	NP_001073315.1:p.Ala1701Asp
NM_004380.2:c.5216C>A	NP_004371.2:p.Ala1739Asp
XM_005255124.3:c.5171C>A	XP_005255181.1:p.Ala1724Asp
XM_005255125.3:c.4799C>A	XP_005255182.1:p.Ala1600Asp
XM_006720848.2:c.4955C>A	XP_006720911.1:p.Ala1652Asp
XM_011522380.1:c.5162C>A	XP_011520682.1:p.Ala1721Asp
XM_011522381.1:c.4463C>A	XP_011520683.1:p.Ala1488Asp
XM_005255124.4:c.5171C>A	XP_005255181.1:p.Ala1724Asp
XM_005255125.4:c.4799C>A	XP_005255182.1:p.Ala1600Asp
XM_006720848.3:c.4955C>A	XP_006720911.1:p.Ala1652Asp
XM_011522381.2:c.4463C>A	XP_011520683.1:p.Ala1488Asp
XM_017022944.1:c.5210C>A	XP_016878433.1:p.Ala1737Asp
NM_004380.3:c.5216C>A MANE Select	NP_004371.2:p.Ala1739Asp