Canonical Allele Identifier: CA394551113

Gene: CREBBP

Linked Data

• ClinVar Variation Id: 2057452
• ClinVar RCV Id: RCV002923367
• dbSNP Id: rs1485287458
• gnomAD v2: 16-3820749-G-A
• gnomAD v3: 16-3770748-G-A
• gnomAD v4: 16-3770748-G-A
• MyVariant Identifiers: chr16:g.3820749G>A (hg19) ; chr16:g.3770748G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3770748G>A , CM000678.2:g.3770748G>A	GRCh38
NC_000016.9:g.3820749G>A , CM000678.1:g.3820749G>A	GRCh37
NC_000016.8:g.3760750G>A	NCBI36
NG_009873.1:g.114373C>T
NG_009873.2:g.114966C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2702C>T MANE Select	ENSP00000262367.5:p.Pro901Leu
ENST00000262367.9:c.2702C>T	ENSP00000262367.5:p.Pro901Leu
ENST00000382070.7:c.2588C>T	ENSP00000371502.3:p.Pro863Leu
ENST00000570939.2:c.1307C>T	ENSP00000461002.2:p.Pro436Leu
NM_001079846.1:c.2588C>T	NP_001073315.1:p.Pro863Leu
NM_004380.2:c.2702C>T	NP_004371.2:p.Pro901Leu
XM_005255124.3:c.2657C>T	XP_005255181.1:p.Pro886Leu
XM_005255125.3:c.2464-1395C>T	XP_005255182.1:n.2464-1395C>T
XM_006720848.2:c.2702C>T	XP_006720911.1:p.Pro901Leu
XM_011522380.1:c.2648C>T	XP_011520682.1:p.Pro883Leu
XM_011522381.1:c.1949C>T	XP_011520683.1:p.Pro650Leu
XM_011522382.1:c.2702C>T	XP_011520684.1:p.Pro901Leu
XM_005255124.4:c.2657C>T	XP_005255181.1:p.Pro886Leu
XM_005255125.4:c.2464-1395C>T	XP_005255182.1:n.2464-1395C>T
XM_006720848.3:c.2702C>T	XP_006720911.1:p.Pro901Leu
XM_011522381.2:c.1949C>T	XP_011520683.1:p.Pro650Leu
XM_011522382.3:c.2702C>T	XP_011520684.1:p.Pro901Leu
XM_017022944.1:c.2696C>T	XP_016878433.1:p.Pro899Leu
NM_004380.3:c.2702C>T MANE Select	NP_004371.2:p.Pro901Leu