Canonical Allele Identifier: CA2631401399

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3736449-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736449T>C , CM000678.2:g.3736449T>C	GRCh38
NC_000016.9:g.3786450T>C , CM000678.1:g.3786450T>C	GRCh37
NC_000016.8:g.3726451T>C	NCBI36
NG_009873.1:g.148672A>G
NG_009873.2:g.149265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4560+201A>G MANE Select	ENSP00000262367.5:n.4560+201A>G
ENST00000262367.9:c.4560+201A>G	ENSP00000262367.5:n.4560+201A>G
ENST00000382070.7:c.4446+201A>G	ENSP00000371502.3:n.4446+201A>G
ENST00000570939.2:c.3195+201A>G	ENSP00000461002.2:n.3195+201A>G
ENST00000571763.5:n.350+201A>G
ENST00000576720.1:n.3383+201A>G
NM_001079846.1:c.4446+201A>G	NP_001073315.1:n.4446+201A>G
NM_004380.2:c.4560+201A>G	NP_004371.2:n.4560+201A>G
XM_005255124.3:c.4515+201A>G	XP_005255181.1:n.4515+201A>G
XM_005255125.3:c.4143+201A>G	XP_005255182.1:n.4143+201A>G
XM_006720848.2:c.4299+201A>G	XP_006720911.1:n.4299+201A>G
XM_011522380.1:c.4506+201A>G	XP_011520682.1:n.4506+201A>G
XM_011522381.1:c.3807+201A>G	XP_011520683.1:n.3807+201A>G
XM_005255124.4:c.4515+201A>G	XP_005255181.1:n.4515+201A>G
XM_005255125.4:c.4143+201A>G	XP_005255182.1:n.4143+201A>G
XM_006720848.3:c.4299+201A>G	XP_006720911.1:n.4299+201A>G
XM_011522381.2:c.3807+201A>G	XP_011520683.1:n.3807+201A>G
XM_017022944.1:c.4554+201A>G	XP_016878433.1:n.4554+201A>G
NM_004380.3:c.4560+201A>G MANE Select	NP_004371.2:n.4560+201A>G