Canonical Allele Identifier: CA493393496

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778040G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728039G>A , CM000678.2:g.3728039G>A	GRCh38
NC_000016.9:g.3778040G>A , CM000678.1:g.3778040G>A	GRCh37
NC_000016.8:g.3718041G>A	NCBI36
NG_009873.1:g.157082C>T
NG_009873.2:g.157675C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7008C>T MANE Select	ENSP00000262367.5:p.Ala2336=
ENST00000262367.9:c.7008C>T	ENSP00000262367.5:p.Ala2336=
ENST00000382070.7:c.6894C>T	ENSP00000371502.3:p.Ala2298=
NM_001079846.1:c.6894C>T	NP_001073315.1:p.Ala2298=
NM_004380.2:c.7008C>T	NP_004371.2:p.Ala2336=
XM_005255124.3:c.6963C>T	XP_005255181.1:p.Ala2321=
XM_005255125.3:c.6591C>T	XP_005255182.1:p.Ala2197=
XM_006720848.2:c.6747C>T	XP_006720911.1:p.Ala2249=
XM_011522380.1:c.6954C>T	XP_011520682.1:p.Ala2318=
XM_011522381.1:c.6255C>T	XP_011520683.1:p.Ala2085=
XM_005255124.4:c.6963C>T	XP_005255181.1:p.Ala2321=
XM_005255125.4:c.6591C>T	XP_005255182.1:p.Ala2197=
XM_006720848.3:c.6747C>T	XP_006720911.1:p.Ala2249=
XM_011522381.2:c.6255C>T	XP_011520683.1:p.Ala2085=
XM_017022944.1:c.7002C>T	XP_016878433.1:p.Ala2334=
NM_004380.3:c.7008C>T MANE Select	NP_004371.2:p.Ala2336=