Canonical Allele Identifier: CA394554121

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778914T>C (hg19) ; chr16:g.3728913T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728913T>C , CM000678.2:g.3728913T>C	GRCh38
NC_000016.9:g.3778914T>C , CM000678.1:g.3778914T>C	GRCh37
NC_000016.8:g.3718915T>C	NCBI36
NG_009873.1:g.156208A>G
NG_009873.2:g.156801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6134A>G MANE Select	ENSP00000262367.5:p.Gln2045Arg
ENST00000262367.9:c.6134A>G	ENSP00000262367.5:p.Gln2045Arg
ENST00000382070.7:c.6020A>G	ENSP00000371502.3:p.Gln2007Arg
NM_001079846.1:c.6020A>G	NP_001073315.1:p.Gln2007Arg
NM_004380.2:c.6134A>G	NP_004371.2:p.Gln2045Arg
XM_005255124.3:c.6089A>G	XP_005255181.1:p.Gln2030Arg
XM_005255125.3:c.5717A>G	XP_005255182.1:p.Gln1906Arg
XM_006720848.2:c.5873A>G	XP_006720911.1:p.Gln1958Arg
XM_011522380.1:c.6080A>G	XP_011520682.1:p.Gln2027Arg
XM_011522381.1:c.5381A>G	XP_011520683.1:p.Gln1794Arg
XM_005255124.4:c.6089A>G	XP_005255181.1:p.Gln2030Arg
XM_005255125.4:c.5717A>G	XP_005255182.1:p.Gln1906Arg
XM_006720848.3:c.5873A>G	XP_006720911.1:p.Gln1958Arg
XM_011522381.2:c.5381A>G	XP_011520683.1:p.Gln1794Arg
XM_017022944.1:c.6128A>G	XP_016878433.1:p.Gln2043Arg
NM_004380.3:c.6134A>G MANE Select	NP_004371.2:p.Gln2045Arg