Canonical Allele Identifier: CA394556600

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779656T>C (hg19) ; chr16:g.3729655T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729655T>C , CM000678.2:g.3729655T>C	GRCh38
NC_000016.9:g.3779656T>C , CM000678.1:g.3779656T>C	GRCh37
NC_000016.8:g.3719657T>C	NCBI36
NG_009873.1:g.155466A>G
NG_009873.2:g.156059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5392A>G MANE Select	ENSP00000262367.5:p.Met1798Val
ENST00000262367.9:c.5392A>G	ENSP00000262367.5:p.Met1798Val
ENST00000382070.7:c.5278A>G	ENSP00000371502.3:p.Met1760Val
NM_001079846.1:c.5278A>G	NP_001073315.1:p.Met1760Val
NM_004380.2:c.5392A>G	NP_004371.2:p.Met1798Val
XM_005255124.3:c.5347A>G	XP_005255181.1:p.Met1783Val
XM_005255125.3:c.4975A>G	XP_005255182.1:p.Met1659Val
XM_006720848.2:c.5131A>G	XP_006720911.1:p.Met1711Val
XM_011522380.1:c.5338A>G	XP_011520682.1:p.Met1780Val
XM_011522381.1:c.4639A>G	XP_011520683.1:p.Met1547Val
XM_005255124.4:c.5347A>G	XP_005255181.1:p.Met1783Val
XM_005255125.4:c.4975A>G	XP_005255182.1:p.Met1659Val
XM_006720848.3:c.5131A>G	XP_006720911.1:p.Met1711Val
XM_011522381.2:c.4639A>G	XP_011520683.1:p.Met1547Val
XM_017022944.1:c.5386A>G	XP_016878433.1:p.Met1796Val
NM_004380.3:c.5392A>G MANE Select	NP_004371.2:p.Met1798Val