Canonical Allele Identifier: CA394550212

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3777797C>G (hg19) ; chr16:g.3727796C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727796C>G , CM000678.2:g.3727796C>G	GRCh38
NC_000016.9:g.3777797C>G , CM000678.1:g.3777797C>G	GRCh37
NC_000016.8:g.3717798C>G	NCBI36
NG_009873.1:g.157325G>C
NG_009873.2:g.157918G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7251G>C MANE Select	ENSP00000262367.5:p.Arg2417Ser
ENST00000262367.9:c.7251G>C	ENSP00000262367.5:p.Arg2417Ser
ENST00000382070.7:c.7137G>C	ENSP00000371502.3:p.Arg2379Ser
NM_001079846.1:c.7137G>C	NP_001073315.1:p.Arg2379Ser
NM_004380.2:c.7251G>C	NP_004371.2:p.Arg2417Ser
XM_005255124.3:c.7206G>C	XP_005255181.1:p.Arg2402Ser
XM_005255125.3:c.6834G>C	XP_005255182.1:p.Arg2278Ser
XM_006720848.2:c.6990G>C	XP_006720911.1:p.Arg2330Ser
XM_011522380.1:c.7197G>C	XP_011520682.1:p.Arg2399Ser
XM_011522381.1:c.6498G>C	XP_011520683.1:p.Arg2166Ser
XM_005255124.4:c.7206G>C	XP_005255181.1:p.Arg2402Ser
XM_005255125.4:c.6834G>C	XP_005255182.1:p.Arg2278Ser
XM_006720848.3:c.6990G>C	XP_006720911.1:p.Arg2330Ser
XM_011522381.2:c.6498G>C	XP_011520683.1:p.Arg2166Ser
XM_017022944.1:c.7245G>C	XP_016878433.1:p.Arg2415Ser
NM_004380.3:c.7251G>C MANE Select	NP_004371.2:p.Arg2417Ser