Canonical Allele Identifier: CA394554016

Gene: CREBBP

Linked Data

• ClinVar Variation Id: 2213598
• ClinVar RCV Id: RCV002665312
• dbSNP Id: rs2151305787
• MyVariant Identifiers: chr16:g.3778887G>A (hg19) ; chr16:g.3728886G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728886G>A , CM000678.2:g.3728886G>A	GRCh38
NC_000016.9:g.3778887G>A , CM000678.1:g.3778887G>A	GRCh37
NC_000016.8:g.3718888G>A	NCBI36
NG_009873.1:g.156235C>T
NG_009873.2:g.156828C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6161C>T MANE Select	ENSP00000262367.5:p.Pro2054Leu
ENST00000262367.9:c.6161C>T	ENSP00000262367.5:p.Pro2054Leu
ENST00000382070.7:c.6047C>T	ENSP00000371502.3:p.Pro2016Leu
NM_001079846.1:c.6047C>T	NP_001073315.1:p.Pro2016Leu
NM_004380.2:c.6161C>T	NP_004371.2:p.Pro2054Leu
XM_005255124.3:c.6116C>T	XP_005255181.1:p.Pro2039Leu
XM_005255125.3:c.5744C>T	XP_005255182.1:p.Pro1915Leu
XM_006720848.2:c.5900C>T	XP_006720911.1:p.Pro1967Leu
XM_011522380.1:c.6107C>T	XP_011520682.1:p.Pro2036Leu
XM_011522381.1:c.5408C>T	XP_011520683.1:p.Pro1803Leu
XM_005255124.4:c.6116C>T	XP_005255181.1:p.Pro2039Leu
XM_005255125.4:c.5744C>T	XP_005255182.1:p.Pro1915Leu
XM_006720848.3:c.5900C>T	XP_006720911.1:p.Pro1967Leu
XM_011522381.2:c.5408C>T	XP_011520683.1:p.Pro1803Leu
XM_017022944.1:c.6155C>T	XP_016878433.1:p.Pro2052Leu
NM_004380.3:c.6161C>T MANE Select	NP_004371.2:p.Pro2054Leu