Canonical Allele Identifier: CA2741462014

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3730103G>C , CM000678.2:g.3730103G>C	GRCh38
NC_000016.9:g.3780104G>C , CM000678.1:g.3780104G>C	GRCh37
NC_000016.8:g.3720105G>C	NCBI36
NG_009873.1:g.155018C>G
NG_009873.2:g.155611C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5173-229C>G MANE Select	ENSP00000262367.5:n.5173-229C>G
ENST00000262367.9:c.5173-229C>G	ENSP00000262367.5:n.5173-229C>G
ENST00000382070.7:c.5059-229C>G	ENSP00000371502.3:n.5059-229C>G
NM_001079846.1:c.5059-229C>G	NP_001073315.1:n.5059-229C>G
NM_004380.2:c.5173-229C>G	NP_004371.2:n.5173-229C>G
XM_005255124.3:c.5128-229C>G	XP_005255181.1:n.5128-229C>G
XM_005255125.3:c.4756-229C>G	XP_005255182.1:n.4756-229C>G
XM_006720848.2:c.4912-229C>G	XP_006720911.1:n.4912-229C>G
XM_011522380.1:c.5119-229C>G	XP_011520682.1:n.5119-229C>G
XM_011522381.1:c.4420-229C>G	XP_011520683.1:n.4420-229C>G
XM_005255124.4:c.5128-229C>G	XP_005255181.1:n.5128-229C>G
XM_005255125.4:c.4756-229C>G	XP_005255182.1:n.4756-229C>G
XM_006720848.3:c.4912-229C>G	XP_006720911.1:n.4912-229C>G
XM_011522381.2:c.4420-229C>G	XP_011520683.1:n.4420-229C>G
XM_017022944.1:c.5167-229C>G	XP_016878433.1:n.5167-229C>G
NM_004380.3:c.5173-229C>G MANE Select	NP_004371.2:n.5173-229C>G