Canonical Allele Identifier: CA394556348

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310698
• MyVariant Identifiers: chr16:g.3779599G>A (hg19) ; chr16:g.3729598G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729598G>A , CM000678.2:g.3729598G>A	GRCh38
NC_000016.9:g.3779599G>A , CM000678.1:g.3779599G>A	GRCh37
NC_000016.8:g.3719600G>A	NCBI36
NG_009873.1:g.155523C>T
NG_009873.2:g.156116C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5449C>T MANE Select	ENSP00000262367.5:p.Pro1817Ser
ENST00000262367.9:c.5449C>T	ENSP00000262367.5:p.Pro1817Ser
ENST00000382070.7:c.5335C>T	ENSP00000371502.3:p.Pro1779Ser
NM_001079846.1:c.5335C>T	NP_001073315.1:p.Pro1779Ser
NM_004380.2:c.5449C>T	NP_004371.2:p.Pro1817Ser
XM_005255124.3:c.5404C>T	XP_005255181.1:p.Pro1802Ser
XM_005255125.3:c.5032C>T	XP_005255182.1:p.Pro1678Ser
XM_006720848.2:c.5188C>T	XP_006720911.1:p.Pro1730Ser
XM_011522380.1:c.5395C>T	XP_011520682.1:p.Pro1799Ser
XM_011522381.1:c.4696C>T	XP_011520683.1:p.Pro1566Ser
XM_005255124.4:c.5404C>T	XP_005255181.1:p.Pro1802Ser
XM_005255125.4:c.5032C>T	XP_005255182.1:p.Pro1678Ser
XM_006720848.3:c.5188C>T	XP_006720911.1:p.Pro1730Ser
XM_011522381.2:c.4696C>T	XP_011520683.1:p.Pro1566Ser
XM_017022944.1:c.5443C>T	XP_016878433.1:p.Pro1815Ser
NM_004380.3:c.5449C>T MANE Select	NP_004371.2:p.Pro1817Ser