Canonical Allele Identifier: CA493393346

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3777953T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727952T>A , CM000678.2:g.3727952T>A	GRCh38
NC_000016.9:g.3777953T>A , CM000678.1:g.3777953T>A	GRCh37
NC_000016.8:g.3717954T>A	NCBI36
NG_009873.1:g.157169A>T
NG_009873.2:g.157762A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7095A>T MANE Select	ENSP00000262367.5:p.Pro2365=
ENST00000262367.9:c.7095A>T	ENSP00000262367.5:p.Pro2365=
ENST00000382070.7:c.6981A>T	ENSP00000371502.3:p.Pro2327=
NM_001079846.1:c.6981A>T	NP_001073315.1:p.Pro2327=
NM_004380.2:c.7095A>T	NP_004371.2:p.Pro2365=
XM_005255124.3:c.7050A>T	XP_005255181.1:p.Pro2350=
XM_005255125.3:c.6678A>T	XP_005255182.1:p.Pro2226=
XM_006720848.2:c.6834A>T	XP_006720911.1:p.Pro2278=
XM_011522380.1:c.7041A>T	XP_011520682.1:p.Pro2347=
XM_011522381.1:c.6342A>T	XP_011520683.1:p.Pro2114=
XM_005255124.4:c.7050A>T	XP_005255181.1:p.Pro2350=
XM_005255125.4:c.6678A>T	XP_005255182.1:p.Pro2226=
XM_006720848.3:c.6834A>T	XP_006720911.1:p.Pro2278=
XM_011522381.2:c.6342A>T	XP_011520683.1:p.Pro2114=
XM_017022944.1:c.7089A>T	XP_016878433.1:p.Pro2363=
NM_004380.3:c.7095A>T MANE Select	NP_004371.2:p.Pro2365=