Canonical Allele Identifier: CA394569531

Gene: CREBBP

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.3316C>T MANE Select	ENSP00000262367.5:p.Pro1106Ser
ENST00000262367.9:c.3316C>T	ENSP00000262367.5:p.Pro1106Ser
ENST00000382070.7:c.3202C>T	ENSP00000371502.3:p.Pro1068Ser
ENST00000570939.2:c.1921C>T	ENSP00000461002.2:p.Pro641Ser
NM_001079846.1:c.3202C>T	NP_001073315.1:p.Pro1068Ser
NM_004380.2:c.3316C>T	NP_004371.2:p.Pro1106Ser
XM_005255124.3:c.3271C>T	XP_005255181.1:p.Pro1091Ser
XM_005255125.3:c.2899C>T	XP_005255182.1:p.Pro967Ser
XM_006720848.2:c.3316C>T	XP_006720911.1:p.Pro1106Ser
XM_011522380.1:c.3262C>T	XP_011520682.1:p.Pro1088Ser
XM_011522381.1:c.2563C>T	XP_011520683.1:p.Pro855Ser
XM_011522382.1:c.3316C>T	XP_011520684.1:p.Pro1106Ser
XM_005255124.4:c.3271C>T	XP_005255181.1:p.Pro1091Ser
XM_005255125.4:c.2899C>T	XP_005255182.1:p.Pro967Ser
XM_006720848.3:c.3316C>T	XP_006720911.1:p.Pro1106Ser
XM_011522381.2:c.2563C>T	XP_011520683.1:p.Pro855Ser
XM_011522382.3:c.3316C>T	XP_011520684.1:p.Pro1106Ser
XM_017022944.1:c.3310C>T	XP_016878433.1:p.Pro1104Ser
NM_004380.3:c.3316C>T MANE Select	NP_004371.2:p.Pro1106Ser