Canonical Allele Identifier: CA394550429

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3777897T>C (hg19) ; chr16:g.3727896T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727896T>C , CM000678.2:g.3727896T>C	GRCh38
NC_000016.9:g.3777897T>C , CM000678.1:g.3777897T>C	GRCh37
NC_000016.8:g.3717898T>C	NCBI36
NG_009873.1:g.157225A>G
NG_009873.2:g.157818A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7151A>G MANE Select	ENSP00000262367.5:p.His2384Arg
ENST00000262367.9:c.7151A>G	ENSP00000262367.5:p.His2384Arg
ENST00000382070.7:c.7037A>G	ENSP00000371502.3:p.His2346Arg
NM_001079846.1:c.7037A>G	NP_001073315.1:p.His2346Arg
NM_004380.2:c.7151A>G	NP_004371.2:p.His2384Arg
XM_005255124.3:c.7106A>G	XP_005255181.1:p.His2369Arg
XM_005255125.3:c.6734A>G	XP_005255182.1:p.His2245Arg
XM_006720848.2:c.6890A>G	XP_006720911.1:p.His2297Arg
XM_011522380.1:c.7097A>G	XP_011520682.1:p.His2366Arg
XM_011522381.1:c.6398A>G	XP_011520683.1:p.His2133Arg
XM_005255124.4:c.7106A>G	XP_005255181.1:p.His2369Arg
XM_005255125.4:c.6734A>G	XP_005255182.1:p.His2245Arg
XM_006720848.3:c.6890A>G	XP_006720911.1:p.His2297Arg
XM_011522381.2:c.6398A>G	XP_011520683.1:p.His2133Arg
XM_017022944.1:c.7145A>G	XP_016878433.1:p.His2382Arg
NM_004380.3:c.7151A>G MANE Select	NP_004371.2:p.His2384Arg