Canonical Allele Identifier: CA394564677

Gene: CREBBP

Linked Data

• COSMIC: COSM1324454
• MyVariant Identifiers: chr16:g.3789578C>A (hg19) ; chr16:g.3739577C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3739577C>A , CM000678.2:g.3739577C>A	GRCh38
NC_000016.9:g.3789578C>A , CM000678.1:g.3789578C>A	GRCh37
NC_000016.8:g.3729579C>A	NCBI36
NG_009873.1:g.145544G>T
NG_009873.2:g.146137G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.4280+1G>T MANE Select	ENSP00000262367.5:n.4280+1G>T
ENST00000262367.9:c.4280+1G>T	ENSP00000262367.5:n.4280+1G>T
ENST00000382070.7:c.4166+1G>T	ENSP00000371502.3:n.4166+1G>T
ENST00000570939.2:c.2915+1G>T	ENSP00000461002.2:n.2915+1G>T
ENST00000573517.6:c.587G>T
ENST00000574740.1:n.215+822G>T
ENST00000576720.1:n.3217+1G>T
NM_001079846.1:c.4166+1G>T	NP_001073315.1:n.4166+1G>T
NM_004380.2:c.4280+1G>T	NP_004371.2:n.4280+1G>T
XM_005255124.3:c.4235+1G>T	XP_005255181.1:n.4235+1G>T
XM_005255125.3:c.3863+1G>T	XP_005255182.1:n.3863+1G>T
XM_006720848.2:c.4133+822G>T	XP_006720911.1:n.4133+822G>T
XM_011522380.1:c.4226+1G>T	XP_011520682.1:n.4226+1G>T
XM_011522381.1:c.3527+1G>T	XP_011520683.1:n.3527+1G>T
XM_005255124.4:c.4235+1G>T	XP_005255181.1:n.4235+1G>T
XM_005255125.4:c.3863+1G>T	XP_005255182.1:n.3863+1G>T
XM_006720848.3:c.4133+822G>T	XP_006720911.1:n.4133+822G>T
XM_011522381.2:c.3527+1G>T	XP_011520683.1:n.3527+1G>T
XM_017022944.1:c.4274+1G>T	XP_016878433.1:n.4274+1G>T
NM_004380.3:c.4280+1G>T MANE Select	NP_004371.2:n.4280+1G>T