Canonical Allele Identifier: CA493276261

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3828043C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778042C>A , CM000678.2:g.3778042C>A	GRCh38
NC_000016.9:g.3828043C>A , CM000678.1:g.3828043C>A	GRCh37
NC_000016.8:g.3768044C>A	NCBI36
NG_009873.1:g.107079G>T
NG_009873.2:g.107672G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2082G>T MANE Select	ENSP00000262367.5:p.Val694=
ENST00000262367.9:c.2082G>T	ENSP00000262367.5:p.Val694=
ENST00000382070.7:c.1968G>T	ENSP00000371502.3:p.Val656=
ENST00000570939.2:c.687G>T	ENSP00000461002.2:p.Val229=
ENST00000571826.5:c.131G>T
ENST00000572134.1:c.395G>T
ENST00000634839.1:n.244G>T
NM_001079846.1:c.1968G>T	NP_001073315.1:p.Val656=
NM_004380.2:c.2082G>T	NP_004371.2:p.Val694=
XM_005255124.3:c.2082G>T	XP_005255181.1:p.Val694=
XM_005255125.3:c.2082G>T	XP_005255182.1:p.Val694=
XM_006720848.2:c.2082G>T	XP_006720911.1:p.Val694=
XM_011522380.1:c.2028G>T	XP_011520682.1:p.Val676=
XM_011522381.1:c.1329G>T	XP_011520683.1:p.Val443=
XM_011522382.1:c.2082G>T	XP_011520684.1:p.Val694=
XM_005255124.4:c.2082G>T	XP_005255181.1:p.Val694=
XM_005255125.4:c.2082G>T	XP_005255182.1:p.Val694=
XM_006720848.3:c.2082G>T	XP_006720911.1:p.Val694=
XM_011522381.2:c.1329G>T	XP_011520683.1:p.Val443=
XM_011522382.3:c.2082G>T	XP_011520684.1:p.Val694=
XM_017022944.1:c.2082G>T	XP_016878433.1:p.Val694=
NM_004380.3:c.2082G>T MANE Select	NP_004371.2:p.Val694=