Canonical Allele Identifier: CA394569533

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3808908G>T (hg19) ; chr16:g.3758907G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3758907G>T , CM000678.2:g.3758907G>T	GRCh38
NC_000016.9:g.3808908G>T , CM000678.1:g.3808908G>T	GRCh37
NC_000016.8:g.3748909G>T	NCBI36
NG_009873.1:g.126214C>A
NG_009873.2:g.126807C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.3316C>A MANE Select	ENSP00000262367.5:p.Pro1106Thr
ENST00000262367.9:c.3316C>A	ENSP00000262367.5:p.Pro1106Thr
ENST00000382070.7:c.3202C>A	ENSP00000371502.3:p.Pro1068Thr
ENST00000570939.2:c.1921C>A	ENSP00000461002.2:p.Pro641Thr
NM_001079846.1:c.3202C>A	NP_001073315.1:p.Pro1068Thr
NM_004380.2:c.3316C>A	NP_004371.2:p.Pro1106Thr
XM_005255124.3:c.3271C>A	XP_005255181.1:p.Pro1091Thr
XM_005255125.3:c.2899C>A	XP_005255182.1:p.Pro967Thr
XM_006720848.2:c.3316C>A	XP_006720911.1:p.Pro1106Thr
XM_011522380.1:c.3262C>A	XP_011520682.1:p.Pro1088Thr
XM_011522381.1:c.2563C>A	XP_011520683.1:p.Pro855Thr
XM_011522382.1:c.3316C>A	XP_011520684.1:p.Pro1106Thr
XM_005255124.4:c.3271C>A	XP_005255181.1:p.Pro1091Thr
XM_005255125.4:c.2899C>A	XP_005255182.1:p.Pro967Thr
XM_006720848.3:c.3316C>A	XP_006720911.1:p.Pro1106Thr
XM_011522381.2:c.2563C>A	XP_011520683.1:p.Pro855Thr
XM_011522382.3:c.3316C>A	XP_011520684.1:p.Pro1106Thr
XM_017022944.1:c.3310C>A	XP_016878433.1:p.Pro1104Thr
NM_004380.3:c.3316C>A MANE Select	NP_004371.2:p.Pro1106Thr