Canonical Allele Identifier: CA394557051

Gene: CREBBP

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729685C>G , CM000678.2:g.3729685C>G	GRCh38
NC_000016.9:g.3779686C>G , CM000678.1:g.3779686C>G	GRCh37
NC_000016.8:g.3719687C>G	NCBI36
NG_009873.1:g.155436G>C
NG_009873.2:g.156029G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5362G>C MANE Select	ENSP00000262367.5:p.Ala1788Pro
ENST00000262367.9:c.5362G>C	ENSP00000262367.5:p.Ala1788Pro
ENST00000382070.7:c.5248G>C	ENSP00000371502.3:p.Ala1750Pro
NM_001079846.1:c.5248G>C	NP_001073315.1:p.Ala1750Pro
NM_004380.2:c.5362G>C	NP_004371.2:p.Ala1788Pro
XM_005255124.3:c.5317G>C	XP_005255181.1:p.Ala1773Pro
XM_005255125.3:c.4945G>C	XP_005255182.1:p.Ala1649Pro
XM_006720848.2:c.5101G>C	XP_006720911.1:p.Ala1701Pro
XM_011522380.1:c.5308G>C	XP_011520682.1:p.Ala1770Pro
XM_011522381.1:c.4609G>C	XP_011520683.1:p.Ala1537Pro
XM_005255124.4:c.5317G>C	XP_005255181.1:p.Ala1773Pro
XM_005255125.4:c.4945G>C	XP_005255182.1:p.Ala1649Pro
XM_006720848.3:c.5101G>C	XP_006720911.1:p.Ala1701Pro
XM_011522381.2:c.4609G>C	XP_011520683.1:p.Ala1537Pro
XM_017022944.1:c.5356G>C	XP_016878433.1:p.Ala1786Pro
NM_004380.3:c.5362G>C MANE Select	NP_004371.2:p.Ala1788Pro