Canonical Allele Identifier: CA2575893793

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3727659-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727659G>A , CM000678.2:g.3727659G>A	GRCh38
NC_000016.9:g.3777660G>A , CM000678.1:g.3777660G>A	GRCh37
NC_000016.8:g.3717661G>A	NCBI36
NG_009873.1:g.157462C>T
NG_009873.2:g.158055C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.*59C>T MANE Select	ENSP00000262367.5:n.*59C>T
ENST00000262367.9:c.*59C>T	ENSP00000262367.5:n.*59C>T
ENST00000382070.7:c.*59C>T	ENSP00000371502.3:n.*59C>T
NM_001079846.1:c.*59C>T	NP_001073315.1:n.*59C>T
NM_004380.2:c.*59C>T	NP_004371.2:n.*59C>T
XM_005255124.3:c.*59C>T	XP_005255181.1:n.*59C>T
XM_005255125.3:c.*59C>T	XP_005255182.1:n.*59C>T
XM_006720848.2:c.*59C>T	XP_006720911.1:n.*59C>T
XM_011522380.1:c.*59C>T	XP_011520682.1:n.*59C>T
XM_011522381.1:c.*59C>T	XP_011520683.1:n.*59C>T
XM_005255124.4:c.*59C>T	XP_005255181.1:n.*59C>T
XM_005255125.4:c.*59C>T	XP_005255182.1:n.*59C>T
XM_006720848.3:c.*59C>T	XP_006720911.1:n.*59C>T
XM_011522381.2:c.*59C>T	XP_011520683.1:n.*59C>T
XM_017022944.1:c.*59C>T	XP_016878433.1:n.*59C>T
NM_004380.3:c.*59C>T MANE Select	NP_004371.2:n.*59C>T