Canonical Allele Identifier: CA493393052

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3777746C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727745C>G , CM000678.2:g.3727745C>G	GRCh38
NC_000016.9:g.3777746C>G , CM000678.1:g.3777746C>G	GRCh37
NC_000016.8:g.3717747C>G	NCBI36
NG_009873.1:g.157376G>C
NG_009873.2:g.157969G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7302G>C MANE Select	ENSP00000262367.5:p.Thr2434=
ENST00000262367.9:c.7302G>C	ENSP00000262367.5:p.Thr2434=
ENST00000382070.7:c.7188G>C	ENSP00000371502.3:p.Thr2396=
NM_001079846.1:c.7188G>C	NP_001073315.1:p.Thr2396=
NM_004380.2:c.7302G>C	NP_004371.2:p.Thr2434=
XM_005255124.3:c.7257G>C	XP_005255181.1:p.Thr2419=
XM_005255125.3:c.6885G>C	XP_005255182.1:p.Thr2295=
XM_006720848.2:c.7041G>C	XP_006720911.1:p.Thr2347=
XM_011522380.1:c.7248G>C	XP_011520682.1:p.Thr2416=
XM_011522381.1:c.6549G>C	XP_011520683.1:p.Thr2183=
XM_005255124.4:c.7257G>C	XP_005255181.1:p.Thr2419=
XM_005255125.4:c.6885G>C	XP_005255182.1:p.Thr2295=
XM_006720848.3:c.7041G>C	XP_006720911.1:p.Thr2347=
XM_011522381.2:c.6549G>C	XP_011520683.1:p.Thr2183=
XM_017022944.1:c.7296G>C	XP_016878433.1:p.Thr2432=
NM_004380.3:c.7302G>C MANE Select	NP_004371.2:p.Thr2434=