Canonical Allele Identifier: CA2631401405

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3736453-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736453G>T , CM000678.2:g.3736453G>T	GRCh38
NC_000016.9:g.3786454G>T , CM000678.1:g.3786454G>T	GRCh37
NC_000016.8:g.3726455G>T	NCBI36
NG_009873.1:g.148668C>A
NG_009873.2:g.149261C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4560+197C>A MANE Select	ENSP00000262367.5:n.4560+197C>A
ENST00000262367.9:c.4560+197C>A	ENSP00000262367.5:n.4560+197C>A
ENST00000382070.7:c.4446+197C>A	ENSP00000371502.3:n.4446+197C>A
ENST00000570939.2:c.3195+197C>A	ENSP00000461002.2:n.3195+197C>A
ENST00000571763.5:n.350+197C>A
ENST00000576720.1:n.3383+197C>A
NM_001079846.1:c.4446+197C>A	NP_001073315.1:n.4446+197C>A
NM_004380.2:c.4560+197C>A	NP_004371.2:n.4560+197C>A
XM_005255124.3:c.4515+197C>A	XP_005255181.1:n.4515+197C>A
XM_005255125.3:c.4143+197C>A	XP_005255182.1:n.4143+197C>A
XM_006720848.2:c.4299+197C>A	XP_006720911.1:n.4299+197C>A
XM_011522380.1:c.4506+197C>A	XP_011520682.1:n.4506+197C>A
XM_011522381.1:c.3807+197C>A	XP_011520683.1:n.3807+197C>A
XM_005255124.4:c.4515+197C>A	XP_005255181.1:n.4515+197C>A
XM_005255125.4:c.4143+197C>A	XP_005255182.1:n.4143+197C>A
XM_006720848.3:c.4299+197C>A	XP_006720911.1:n.4299+197C>A
XM_011522381.2:c.3807+197C>A	XP_011520683.1:n.3807+197C>A
XM_017022944.1:c.4554+197C>A	XP_016878433.1:n.4554+197C>A
NM_004380.3:c.4560+197C>A MANE Select	NP_004371.2:n.4560+197C>A