Canonical Allele Identifier: CA493393041

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778136C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728135C>T , CM000678.2:g.3728135C>T	GRCh38
NC_000016.9:g.3778136C>T , CM000678.1:g.3778136C>T	GRCh37
NC_000016.8:g.3718137C>T	NCBI36
NG_009873.1:g.156986G>A
NG_009873.2:g.157579G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6912G>A MANE Select	ENSP00000262367.5:p.Gln2304=
ENST00000262367.9:c.6912G>A	ENSP00000262367.5:p.Gln2304=
ENST00000382070.7:c.6798G>A	ENSP00000371502.3:p.Gln2266=
NM_001079846.1:c.6798G>A	NP_001073315.1:p.Gln2266=
NM_004380.2:c.6912G>A	NP_004371.2:p.Gln2304=
XM_005255124.3:c.6867G>A	XP_005255181.1:p.Gln2289=
XM_005255125.3:c.6495G>A	XP_005255182.1:p.Gln2165=
XM_006720848.2:c.6651G>A	XP_006720911.1:p.Gln2217=
XM_011522380.1:c.6858G>A	XP_011520682.1:p.Gln2286=
XM_011522381.1:c.6159G>A	XP_011520683.1:p.Gln2053=
XM_005255124.4:c.6867G>A	XP_005255181.1:p.Gln2289=
XM_005255125.4:c.6495G>A	XP_005255182.1:p.Gln2165=
XM_006720848.3:c.6651G>A	XP_006720911.1:p.Gln2217=
XM_011522381.2:c.6159G>A	XP_011520683.1:p.Gln2053=
XM_017022944.1:c.6906G>A	XP_016878433.1:p.Gln2302=
NM_004380.3:c.6912G>A MANE Select	NP_004371.2:p.Gln2304=