Canonical Allele Identifier: CA394556412

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310825
• MyVariant Identifiers: chr16:g.3779613G>A (hg19) ; chr16:g.3729612G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729612G>A , CM000678.2:g.3729612G>A	GRCh38
NC_000016.9:g.3779613G>A , CM000678.1:g.3779613G>A	GRCh37
NC_000016.8:g.3719614G>A	NCBI36
NG_009873.1:g.155509C>T
NG_009873.2:g.156102C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5435C>T MANE Select	ENSP00000262367.5:p.Thr1812Ile
ENST00000262367.9:c.5435C>T	ENSP00000262367.5:p.Thr1812Ile
ENST00000382070.7:c.5321C>T	ENSP00000371502.3:p.Thr1774Ile
NM_001079846.1:c.5321C>T	NP_001073315.1:p.Thr1774Ile
NM_004380.2:c.5435C>T	NP_004371.2:p.Thr1812Ile
XM_005255124.3:c.5390C>T	XP_005255181.1:p.Thr1797Ile
XM_005255125.3:c.5018C>T	XP_005255182.1:p.Thr1673Ile
XM_006720848.2:c.5174C>T	XP_006720911.1:p.Thr1725Ile
XM_011522380.1:c.5381C>T	XP_011520682.1:p.Thr1794Ile
XM_011522381.1:c.4682C>T	XP_011520683.1:p.Thr1561Ile
XM_005255124.4:c.5390C>T	XP_005255181.1:p.Thr1797Ile
XM_005255125.4:c.5018C>T	XP_005255182.1:p.Thr1673Ile
XM_006720848.3:c.5174C>T	XP_006720911.1:p.Thr1725Ile
XM_011522381.2:c.4682C>T	XP_011520683.1:p.Thr1561Ile
XM_017022944.1:c.5429C>T	XP_016878433.1:p.Thr1810Ile
NM_004380.3:c.5435C>T MANE Select	NP_004371.2:p.Thr1812Ile