Canonical Allele Identifier: CA394554450

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3778067-G-T
• MyVariant Identifiers: chr16:g.3828068G>T (hg19) ; chr16:g.3778067G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778067G>T , CM000678.2:g.3778067G>T	GRCh38
NC_000016.9:g.3828068G>T , CM000678.1:g.3828068G>T	GRCh37
NC_000016.8:g.3768069G>T	NCBI36
NG_009873.1:g.107054C>A
NG_009873.2:g.107647C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2057C>A MANE Select	ENSP00000262367.5:p.Pro686Gln
ENST00000262367.9:c.2057C>A	ENSP00000262367.5:p.Pro686Gln
ENST00000382070.7:c.1943C>A	ENSP00000371502.3:p.Pro648Gln
ENST00000570939.2:c.662C>A	ENSP00000461002.2:p.Pro221Gln
ENST00000571826.5:c.106C>A
ENST00000572134.1:c.370C>A
ENST00000634839.1:n.219C>A
NM_001079846.1:c.1943C>A	NP_001073315.1:p.Pro648Gln
NM_004380.2:c.2057C>A	NP_004371.2:p.Pro686Gln
XM_005255124.3:c.2057C>A	XP_005255181.1:p.Pro686Gln
XM_005255125.3:c.2057C>A	XP_005255182.1:p.Pro686Gln
XM_006720848.2:c.2057C>A	XP_006720911.1:p.Pro686Gln
XM_011522380.1:c.2003C>A	XP_011520682.1:p.Pro668Gln
XM_011522381.1:c.1304C>A	XP_011520683.1:p.Pro435Gln
XM_011522382.1:c.2057C>A	XP_011520684.1:p.Pro686Gln
XM_005255124.4:c.2057C>A	XP_005255181.1:p.Pro686Gln
XM_005255125.4:c.2057C>A	XP_005255182.1:p.Pro686Gln
XM_006720848.3:c.2057C>A	XP_006720911.1:p.Pro686Gln
XM_011522381.2:c.1304C>A	XP_011520683.1:p.Pro435Gln
XM_011522382.3:c.2057C>A	XP_011520684.1:p.Pro686Gln
XM_017022944.1:c.2057C>A	XP_016878433.1:p.Pro686Gln
NM_004380.3:c.2057C>A MANE Select	NP_004371.2:p.Pro686Gln