Canonical Allele Identifier: CA271365

Gene: CREBBP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3850931T>C , CM000678.2:g.3850931T>C	GRCh38
NC_000016.9:g.3900932T>C , CM000678.1:g.3900932T>C	GRCh37
NC_000016.8:g.3840933T>C	NCBI36
NG_009873.1:g.34190A>G
NG_009873.2:g.34783A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.164A>G MANE Select	ENSP00000262367.5:p.Asn55Ser
ENST00000262367.9:c.164A>G	ENSP00000262367.5:p.Asn55Ser
ENST00000382070.7:c.164A>G	ENSP00000371502.3:p.Asn55Ser
NM_001079846.1:c.164A>G	NP_001073315.1:p.Asn55Ser
NM_004380.2:c.164A>G	NP_004371.2:p.Asn55Ser
XM_005255124.3:c.164A>G	XP_005255181.1:p.Asn55Ser
XM_005255125.3:c.164A>G	XP_005255182.1:p.Asn55Ser
XM_006720848.2:c.164A>G	XP_006720911.1:p.Asn55Ser
XM_011522380.1:c.110A>G	XP_011520682.1:p.Asn37Ser
XM_011522382.1:c.164A>G	XP_011520684.1:p.Asn55Ser
XM_005255124.4:c.164A>G	XP_005255181.1:p.Asn55Ser
XM_005255125.4:c.164A>G	XP_005255182.1:p.Asn55Ser
XM_006720848.3:c.164A>G	XP_006720911.1:p.Asn55Ser
XM_011522382.3:c.164A>G	XP_011520684.1:p.Asn55Ser
XM_017022944.1:c.164A>G	XP_016878433.1:p.Asn55Ser
NM_004380.3:c.164A>G MANE Select	NP_004371.2:p.Asn55Ser