Canonical Allele Identifier: CA394557127

Gene: CREBBP

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729711A>T , CM000678.2:g.3729711A>T	GRCh38
NC_000016.9:g.3779712A>T , CM000678.1:g.3779712A>T	GRCh37
NC_000016.8:g.3719713A>T	NCBI36
NG_009873.1:g.155410T>A
NG_009873.2:g.156003T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5336T>A MANE Select	ENSP00000262367.5:p.Leu1779Gln
ENST00000262367.9:c.5336T>A	ENSP00000262367.5:p.Leu1779Gln
ENST00000382070.7:c.5222T>A	ENSP00000371502.3:p.Leu1741Gln
NM_001079846.1:c.5222T>A	NP_001073315.1:p.Leu1741Gln
NM_004380.2:c.5336T>A	NP_004371.2:p.Leu1779Gln
XM_005255124.3:c.5291T>A	XP_005255181.1:p.Leu1764Gln
XM_005255125.3:c.4919T>A	XP_005255182.1:p.Leu1640Gln
XM_006720848.2:c.5075T>A	XP_006720911.1:p.Leu1692Gln
XM_011522380.1:c.5282T>A	XP_011520682.1:p.Leu1761Gln
XM_011522381.1:c.4583T>A	XP_011520683.1:p.Leu1528Gln
XM_005255124.4:c.5291T>A	XP_005255181.1:p.Leu1764Gln
XM_005255125.4:c.4919T>A	XP_005255182.1:p.Leu1640Gln
XM_006720848.3:c.5075T>A	XP_006720911.1:p.Leu1692Gln
XM_011522381.2:c.4583T>A	XP_011520683.1:p.Leu1528Gln
XM_017022944.1:c.5330T>A	XP_016878433.1:p.Leu1777Gln
NM_004380.3:c.5336T>A MANE Select	NP_004371.2:p.Leu1779Gln