Canonical Allele Identifier: CA394556608

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151311206
• MyVariant Identifiers: chr16:g.3779658T>A (hg19) ; chr16:g.3729657T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729657T>A , CM000678.2:g.3729657T>A	GRCh38
NC_000016.9:g.3779658T>A , CM000678.1:g.3779658T>A	GRCh37
NC_000016.8:g.3719659T>A	NCBI36
NG_009873.1:g.155464A>T
NG_009873.2:g.156057A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5390A>T MANE Select	ENSP00000262367.5:p.Lys1797Met
ENST00000262367.9:c.5390A>T	ENSP00000262367.5:p.Lys1797Met
ENST00000382070.7:c.5276A>T	ENSP00000371502.3:p.Lys1759Met
NM_001079846.1:c.5276A>T	NP_001073315.1:p.Lys1759Met
NM_004380.2:c.5390A>T	NP_004371.2:p.Lys1797Met
XM_005255124.3:c.5345A>T	XP_005255181.1:p.Lys1782Met
XM_005255125.3:c.4973A>T	XP_005255182.1:p.Lys1658Met
XM_006720848.2:c.5129A>T	XP_006720911.1:p.Lys1710Met
XM_011522380.1:c.5336A>T	XP_011520682.1:p.Lys1779Met
XM_011522381.1:c.4637A>T	XP_011520683.1:p.Lys1546Met
XM_005255124.4:c.5345A>T	XP_005255181.1:p.Lys1782Met
XM_005255125.4:c.4973A>T	XP_005255182.1:p.Lys1658Met
XM_006720848.3:c.5129A>T	XP_006720911.1:p.Lys1710Met
XM_011522381.2:c.4637A>T	XP_011520683.1:p.Lys1546Met
XM_017022944.1:c.5384A>T	XP_016878433.1:p.Lys1795Met
NM_004380.3:c.5390A>T MANE Select	NP_004371.2:p.Lys1797Met