Canonical Allele Identifier: CA394556049

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310008
• MyVariant Identifiers: chr16:g.3779502T>G (hg19) ; chr16:g.3729501T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729501T>G , CM000678.2:g.3729501T>G	GRCh38
NC_000016.9:g.3779502T>G , CM000678.1:g.3779502T>G	GRCh37
NC_000016.8:g.3719503T>G	NCBI36
NG_009873.1:g.155620A>C
NG_009873.2:g.156213A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5546A>C MANE Select	ENSP00000262367.5:p.Lys1849Thr
ENST00000262367.9:c.5546A>C	ENSP00000262367.5:p.Lys1849Thr
ENST00000382070.7:c.5432A>C	ENSP00000371502.3:p.Lys1811Thr
NM_001079846.1:c.5432A>C	NP_001073315.1:p.Lys1811Thr
NM_004380.2:c.5546A>C	NP_004371.2:p.Lys1849Thr
XM_005255124.3:c.5501A>C	XP_005255181.1:p.Lys1834Thr
XM_005255125.3:c.5129A>C	XP_005255182.1:p.Lys1710Thr
XM_006720848.2:c.5285A>C	XP_006720911.1:p.Lys1762Thr
XM_011522380.1:c.5492A>C	XP_011520682.1:p.Lys1831Thr
XM_011522381.1:c.4793A>C	XP_011520683.1:p.Lys1598Thr
XM_005255124.4:c.5501A>C	XP_005255181.1:p.Lys1834Thr
XM_005255125.4:c.5129A>C	XP_005255182.1:p.Lys1710Thr
XM_006720848.3:c.5285A>C	XP_006720911.1:p.Lys1762Thr
XM_011522381.2:c.4793A>C	XP_011520683.1:p.Lys1598Thr
XM_017022944.1:c.5540A>C	XP_016878433.1:p.Lys1847Thr
NM_004380.3:c.5546A>C MANE Select	NP_004371.2:p.Lys1849Thr