Canonical Allele Identifier: CA394557217

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779734T>C (hg19) ; chr16:g.3729733T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729733T>C , CM000678.2:g.3729733T>C	GRCh38
NC_000016.9:g.3779734T>C , CM000678.1:g.3779734T>C	GRCh37
NC_000016.8:g.3719735T>C	NCBI36
NG_009873.1:g.155388A>G
NG_009873.2:g.155981A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5314A>G MANE Select	ENSP00000262367.5:p.Ile1772Val
ENST00000262367.9:c.5314A>G	ENSP00000262367.5:p.Ile1772Val
ENST00000382070.7:c.5200A>G	ENSP00000371502.3:p.Ile1734Val
NM_001079846.1:c.5200A>G	NP_001073315.1:p.Ile1734Val
NM_004380.2:c.5314A>G	NP_004371.2:p.Ile1772Val
XM_005255124.3:c.5269A>G	XP_005255181.1:p.Ile1757Val
XM_005255125.3:c.4897A>G	XP_005255182.1:p.Ile1633Val
XM_006720848.2:c.5053A>G	XP_006720911.1:p.Ile1685Val
XM_011522380.1:c.5260A>G	XP_011520682.1:p.Ile1754Val
XM_011522381.1:c.4561A>G	XP_011520683.1:p.Ile1521Val
XM_005255124.4:c.5269A>G	XP_005255181.1:p.Ile1757Val
XM_005255125.4:c.4897A>G	XP_005255182.1:p.Ile1633Val
XM_006720848.3:c.5053A>G	XP_006720911.1:p.Ile1685Val
XM_011522381.2:c.4561A>G	XP_011520683.1:p.Ile1521Val
XM_017022944.1:c.5308A>G	XP_016878433.1:p.Ile1770Val
NM_004380.3:c.5314A>G MANE Select	NP_004371.2:p.Ile1772Val