Canonical Allele Identifier: CA394557130

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779713G>T (hg19) ; chr16:g.3729712G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729712G>T , CM000678.2:g.3729712G>T	GRCh38
NC_000016.9:g.3779713G>T , CM000678.1:g.3779713G>T	GRCh37
NC_000016.8:g.3719714G>T	NCBI36
NG_009873.1:g.155409C>A
NG_009873.2:g.156002C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5335C>A MANE Select	ENSP00000262367.5:p.Leu1779Met
ENST00000262367.9:c.5335C>A	ENSP00000262367.5:p.Leu1779Met
ENST00000382070.7:c.5221C>A	ENSP00000371502.3:p.Leu1741Met
NM_001079846.1:c.5221C>A	NP_001073315.1:p.Leu1741Met
NM_004380.2:c.5335C>A	NP_004371.2:p.Leu1779Met
XM_005255124.3:c.5290C>A	XP_005255181.1:p.Leu1764Met
XM_005255125.3:c.4918C>A	XP_005255182.1:p.Leu1640Met
XM_006720848.2:c.5074C>A	XP_006720911.1:p.Leu1692Met
XM_011522380.1:c.5281C>A	XP_011520682.1:p.Leu1761Met
XM_011522381.1:c.4582C>A	XP_011520683.1:p.Leu1528Met
XM_005255124.4:c.5290C>A	XP_005255181.1:p.Leu1764Met
XM_005255125.4:c.4918C>A	XP_005255182.1:p.Leu1640Met
XM_006720848.3:c.5074C>A	XP_006720911.1:p.Leu1692Met
XM_011522381.2:c.4582C>A	XP_011520683.1:p.Leu1528Met
XM_017022944.1:c.5329C>A	XP_016878433.1:p.Leu1777Met
NM_004380.3:c.5335C>A MANE Select	NP_004371.2:p.Leu1779Met