Canonical Allele Identifier: CA394557157

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779721A>C (hg19) ; chr16:g.3729720A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729720A>C , CM000678.2:g.3729720A>C	GRCh38
NC_000016.9:g.3779721A>C , CM000678.1:g.3779721A>C	GRCh37
NC_000016.8:g.3719722A>C	NCBI36
NG_009873.1:g.155401T>G
NG_009873.2:g.155994T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5327T>G MANE Select	ENSP00000262367.5:p.Ile1776Ser
ENST00000262367.9:c.5327T>G	ENSP00000262367.5:p.Ile1776Ser
ENST00000382070.7:c.5213T>G	ENSP00000371502.3:p.Ile1738Ser
NM_001079846.1:c.5213T>G	NP_001073315.1:p.Ile1738Ser
NM_004380.2:c.5327T>G	NP_004371.2:p.Ile1776Ser
XM_005255124.3:c.5282T>G	XP_005255181.1:p.Ile1761Ser
XM_005255125.3:c.4910T>G	XP_005255182.1:p.Ile1637Ser
XM_006720848.2:c.5066T>G	XP_006720911.1:p.Ile1689Ser
XM_011522380.1:c.5273T>G	XP_011520682.1:p.Ile1758Ser
XM_011522381.1:c.4574T>G	XP_011520683.1:p.Ile1525Ser
XM_005255124.4:c.5282T>G	XP_005255181.1:p.Ile1761Ser
XM_005255125.4:c.4910T>G	XP_005255182.1:p.Ile1637Ser
XM_006720848.3:c.5066T>G	XP_006720911.1:p.Ile1689Ser
XM_011522381.2:c.4574T>G	XP_011520683.1:p.Ile1525Ser
XM_017022944.1:c.5321T>G	XP_016878433.1:p.Ile1774Ser
NM_004380.3:c.5327T>G MANE Select	NP_004371.2:p.Ile1776Ser