Canonical Allele Identifier: CA394556355

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310725
• MyVariant Identifiers: chr16:g.3779601C>G (hg19) ; chr16:g.3729600C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729600C>G , CM000678.2:g.3729600C>G	GRCh38
NC_000016.9:g.3779601C>G , CM000678.1:g.3779601C>G	GRCh37
NC_000016.8:g.3719602C>G	NCBI36
NG_009873.1:g.155521G>C
NG_009873.2:g.156114G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5447G>C MANE Select	ENSP00000262367.5:p.Cys1816Ser
ENST00000262367.9:c.5447G>C	ENSP00000262367.5:p.Cys1816Ser
ENST00000382070.7:c.5333G>C	ENSP00000371502.3:p.Cys1778Ser
NM_001079846.1:c.5333G>C	NP_001073315.1:p.Cys1778Ser
NM_004380.2:c.5447G>C	NP_004371.2:p.Cys1816Ser
XM_005255124.3:c.5402G>C	XP_005255181.1:p.Cys1801Ser
XM_005255125.3:c.5030G>C	XP_005255182.1:p.Cys1677Ser
XM_006720848.2:c.5186G>C	XP_006720911.1:p.Cys1729Ser
XM_011522380.1:c.5393G>C	XP_011520682.1:p.Cys1798Ser
XM_011522381.1:c.4694G>C	XP_011520683.1:p.Cys1565Ser
XM_005255124.4:c.5402G>C	XP_005255181.1:p.Cys1801Ser
XM_005255125.4:c.5030G>C	XP_005255182.1:p.Cys1677Ser
XM_006720848.3:c.5186G>C	XP_006720911.1:p.Cys1729Ser
XM_011522381.2:c.4694G>C	XP_011520683.1:p.Cys1565Ser
XM_017022944.1:c.5441G>C	XP_016878433.1:p.Cys1814Ser
NM_004380.3:c.5447G>C MANE Select	NP_004371.2:p.Cys1816Ser