Canonical Allele Identifier: CA394562207

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3843404G>A (hg19) ; chr16:g.3793403G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3793403G>A , CM000678.2:g.3793403G>A	GRCh38
NC_000016.9:g.3843404G>A , CM000678.1:g.3843404G>A	GRCh37
NC_000016.8:g.3783405G>A	NCBI36
NG_009873.1:g.91718C>T
NG_009873.2:g.92311C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.1199C>T MANE Select	ENSP00000262367.5:p.Ala400Val
ENST00000262367.9:c.1199C>T	ENSP00000262367.5:p.Ala400Val
ENST00000382070.7:c.1199C>T	ENSP00000371502.3:p.Ala400Val
NM_001079846.1:c.1199C>T	NP_001073315.1:p.Ala400Val
NM_004380.2:c.1199C>T	NP_004371.2:p.Ala400Val
XM_005255124.3:c.1199C>T	XP_005255181.1:p.Ala400Val
XM_005255125.3:c.1199C>T	XP_005255182.1:p.Ala400Val
XM_006720848.2:c.1199C>T	XP_006720911.1:p.Ala400Val
XM_011522380.1:c.1145C>T	XP_011520682.1:p.Ala382Val
XM_011522381.1:c.446C>T	XP_011520683.1:p.Ala149Val
XM_011522382.1:c.1199C>T	XP_011520684.1:p.Ala400Val
XM_005255124.4:c.1199C>T	XP_005255181.1:p.Ala400Val
XM_005255125.4:c.1199C>T	XP_005255182.1:p.Ala400Val
XM_006720848.3:c.1199C>T	XP_006720911.1:p.Ala400Val
XM_011522381.2:c.446C>T	XP_011520683.1:p.Ala149Val
XM_011522382.3:c.1199C>T	XP_011520684.1:p.Ala400Val
XM_017022944.1:c.1199C>T	XP_016878433.1:p.Ala400Val
NM_004380.3:c.1199C>T MANE Select	NP_004371.2:p.Ala400Val