Canonical Allele Identifier: CA394556155

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310289
• MyVariant Identifiers: chr16:g.3779539T>C (hg19) ; chr16:g.3729538T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729538T>C , CM000678.2:g.3729538T>C	GRCh38
NC_000016.9:g.3779539T>C , CM000678.1:g.3779539T>C	GRCh37
NC_000016.8:g.3719540T>C	NCBI36
NG_009873.1:g.155583A>G
NG_009873.2:g.156176A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5509A>G MANE Select	ENSP00000262367.5:p.Lys1837Glu
ENST00000262367.9:c.5509A>G	ENSP00000262367.5:p.Lys1837Glu
ENST00000382070.7:c.5395A>G	ENSP00000371502.3:p.Lys1799Glu
NM_001079846.1:c.5395A>G	NP_001073315.1:p.Lys1799Glu
NM_004380.2:c.5509A>G	NP_004371.2:p.Lys1837Glu
XM_005255124.3:c.5464A>G	XP_005255181.1:p.Lys1822Glu
XM_005255125.3:c.5092A>G	XP_005255182.1:p.Lys1698Glu
XM_006720848.2:c.5248A>G	XP_006720911.1:p.Lys1750Glu
XM_011522380.1:c.5455A>G	XP_011520682.1:p.Lys1819Glu
XM_011522381.1:c.4756A>G	XP_011520683.1:p.Lys1586Glu
XM_005255124.4:c.5464A>G	XP_005255181.1:p.Lys1822Glu
XM_005255125.4:c.5092A>G	XP_005255182.1:p.Lys1698Glu
XM_006720848.3:c.5248A>G	XP_006720911.1:p.Lys1750Glu
XM_011522381.2:c.4756A>G	XP_011520683.1:p.Lys1586Glu
XM_017022944.1:c.5503A>G	XP_016878433.1:p.Lys1835Glu
NM_004380.3:c.5509A>G MANE Select	NP_004371.2:p.Lys1837Glu