Canonical Allele Identifier: CA394566046

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3860701A>C (hg19) ; chr16:g.3810700A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3810700A>C , CM000678.2:g.3810700A>C	GRCh38
NC_000016.9:g.3860701A>C , CM000678.1:g.3860701A>C	GRCh37
NC_000016.8:g.3800702A>C	NCBI36
NG_009873.1:g.74421T>G
NG_009873.2:g.75014T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.878T>G MANE Select	ENSP00000262367.5:p.Val293Gly
ENST00000262367.9:c.878T>G	ENSP00000262367.5:p.Val293Gly
ENST00000382070.7:c.878T>G	ENSP00000371502.3:p.Val293Gly
NM_001079846.1:c.878T>G	NP_001073315.1:p.Val293Gly
NM_004380.2:c.878T>G	NP_004371.2:p.Val293Gly
XM_005255124.3:c.878T>G	XP_005255181.1:p.Val293Gly
XM_005255125.3:c.878T>G	XP_005255182.1:p.Val293Gly
XM_006720848.2:c.878T>G	XP_006720911.1:p.Val293Gly
XM_011522380.1:c.824T>G	XP_011520682.1:p.Val275Gly
XM_011522381.1:c.125T>G	XP_011520683.1:p.Val42Gly
XM_011522382.1:c.878T>G	XP_011520684.1:p.Val293Gly
XM_005255124.4:c.878T>G	XP_005255181.1:p.Val293Gly
XM_005255125.4:c.878T>G	XP_005255182.1:p.Val293Gly
XM_006720848.3:c.878T>G	XP_006720911.1:p.Val293Gly
XM_011522381.2:c.125T>G	XP_011520683.1:p.Val42Gly
XM_011522382.3:c.878T>G	XP_011520684.1:p.Val293Gly
XM_017022944.1:c.878T>G	XP_016878433.1:p.Val293Gly
NM_004380.3:c.878T>G MANE Select	NP_004371.2:p.Val293Gly