Canonical Allele Identifier: CA394564050

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151330200
• MyVariant Identifiers: chr16:g.3786815A>C (hg19) ; chr16:g.3736814A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736814A>C , CM000678.2:g.3736814A>C	GRCh38
NC_000016.9:g.3786815A>C , CM000678.1:g.3786815A>C	GRCh37
NC_000016.8:g.3726816A>C	NCBI36
NG_009873.1:g.148307T>G
NG_009873.2:g.148900T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4396T>G MANE Select	ENSP00000262367.5:p.Tyr1466Asp
ENST00000262367.9:c.4396T>G	ENSP00000262367.5:p.Tyr1466Asp
ENST00000382070.7:c.4282T>G	ENSP00000371502.3:p.Tyr1428Asp
ENST00000570939.2:c.3031T>G	ENSP00000461002.2:p.Tyr1011Asp
ENST00000571763.5:n.186T>G
ENST00000574740.1:n.217T>G
ENST00000576720.1:n.3219T>G
NM_001079846.1:c.4282T>G	NP_001073315.1:p.Tyr1428Asp
NM_004380.2:c.4396T>G	NP_004371.2:p.Tyr1466Asp
XM_005255124.3:c.4351T>G	XP_005255181.1:p.Tyr1451Asp
XM_005255125.3:c.3979T>G	XP_005255182.1:p.Tyr1327Asp
XM_006720848.2:c.4135T>G	XP_006720911.1:p.Tyr1379Asp
XM_011522380.1:c.4342T>G	XP_011520682.1:p.Tyr1448Asp
XM_011522381.1:c.3643T>G	XP_011520683.1:p.Tyr1215Asp
XM_005255124.4:c.4351T>G	XP_005255181.1:p.Tyr1451Asp
XM_005255125.4:c.3979T>G	XP_005255182.1:p.Tyr1327Asp
XM_006720848.3:c.4135T>G	XP_006720911.1:p.Tyr1379Asp
XM_011522381.2:c.3643T>G	XP_011520683.1:p.Tyr1215Asp
XM_017022944.1:c.4390T>G	XP_016878433.1:p.Tyr1464Asp
NM_004380.3:c.4396T>G MANE Select	NP_004371.2:p.Tyr1466Asp