Canonical Allele Identifier: CA394565309

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3740451-C-T
• MyVariant Identifiers: chr16:g.3790452C>T (hg19) ; chr16:g.3740451C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3740451C>T , CM000678.2:g.3740451C>T	GRCh38
NC_000016.9:g.3790452C>T , CM000678.1:g.3790452C>T	GRCh37
NC_000016.8:g.3730453C>T	NCBI36
NG_009873.1:g.144670G>A
NG_009873.2:g.145263G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.4081G>A MANE Select	ENSP00000262367.5:p.Val1361Met
ENST00000262367.9:c.4081G>A	ENSP00000262367.5:p.Val1361Met
ENST00000382070.7:c.3967G>A	ENSP00000371502.3:p.Val1323Met
ENST00000570939.2:c.2716G>A	ENSP00000461002.2:p.Val906Met
ENST00000572569.1:n.545G>A
ENST00000573517.6:c.387G>A
ENST00000574740.1:n.163G>A
ENST00000576720.1:n.3018G>A
NM_001079846.1:c.3967G>A	NP_001073315.1:p.Val1323Met
NM_004380.2:c.4081G>A	NP_004371.2:p.Val1361Met
XM_005255124.3:c.4036G>A	XP_005255181.1:p.Val1346Met
XM_005255125.3:c.3664G>A	XP_005255182.1:p.Val1222Met
XM_006720848.2:c.4081G>A	XP_006720911.1:p.Val1361Met
XM_011522380.1:c.4027G>A	XP_011520682.1:p.Val1343Met
XM_011522381.1:c.3328G>A	XP_011520683.1:p.Val1110Met
XM_005255124.4:c.4036G>A	XP_005255181.1:p.Val1346Met
XM_005255125.4:c.3664G>A	XP_005255182.1:p.Val1222Met
XM_006720848.3:c.4081G>A	XP_006720911.1:p.Val1361Met
XM_011522381.2:c.3328G>A	XP_011520683.1:p.Val1110Met
XM_017022944.1:c.4075G>A	XP_016878433.1:p.Val1359Met
NM_004380.3:c.4081G>A MANE Select	NP_004371.2:p.Val1361Met