Canonical Allele Identifier: CA394563468

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3786688T>C (hg19) ; chr16:g.3736687T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736687T>C , CM000678.2:g.3736687T>C	GRCh38
NC_000016.9:g.3786688T>C , CM000678.1:g.3786688T>C	GRCh37
NC_000016.8:g.3726689T>C	NCBI36
NG_009873.1:g.148434A>G
NG_009873.2:g.149027A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4523A>G MANE Select	ENSP00000262367.5:p.Asp1508Gly
ENST00000262367.9:c.4523A>G	ENSP00000262367.5:p.Asp1508Gly
ENST00000382070.7:c.4409A>G	ENSP00000371502.3:p.Asp1470Gly
ENST00000570939.2:c.3158A>G	ENSP00000461002.2:p.Asp1053Gly
ENST00000571763.5:n.313A>G
ENST00000574740.1:n.344A>G
ENST00000576720.1:n.3346A>G
NM_001079846.1:c.4409A>G	NP_001073315.1:p.Asp1470Gly
NM_004380.2:c.4523A>G	NP_004371.2:p.Asp1508Gly
XM_005255124.3:c.4478A>G	XP_005255181.1:p.Asp1493Gly
XM_005255125.3:c.4106A>G	XP_005255182.1:p.Asp1369Gly
XM_006720848.2:c.4262A>G	XP_006720911.1:p.Asp1421Gly
XM_011522380.1:c.4469A>G	XP_011520682.1:p.Asp1490Gly
XM_011522381.1:c.3770A>G	XP_011520683.1:p.Asp1257Gly
XM_005255124.4:c.4478A>G	XP_005255181.1:p.Asp1493Gly
XM_005255125.4:c.4106A>G	XP_005255182.1:p.Asp1369Gly
XM_006720848.3:c.4262A>G	XP_006720911.1:p.Asp1421Gly
XM_011522381.2:c.3770A>G	XP_011520683.1:p.Asp1257Gly
XM_017022944.1:c.4517A>G	XP_016878433.1:p.Asp1506Gly
NM_004380.3:c.4523A>G MANE Select	NP_004371.2:p.Asp1508Gly