Canonical Allele Identifier: CA394563335

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151329174
• MyVariant Identifiers: chr16:g.3786665T>A (hg19) ; chr16:g.3736664T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736664T>A , CM000678.2:g.3736664T>A	GRCh38
NC_000016.9:g.3786665T>A , CM000678.1:g.3786665T>A	GRCh37
NC_000016.8:g.3726666T>A	NCBI36
NG_009873.1:g.148457A>T
NG_009873.2:g.149050A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4546A>T MANE Select	ENSP00000262367.5:p.Ile1516Phe
ENST00000262367.9:c.4546A>T	ENSP00000262367.5:p.Ile1516Phe
ENST00000382070.7:c.4432A>T	ENSP00000371502.3:p.Ile1478Phe
ENST00000570939.2:c.3181A>T	ENSP00000461002.2:p.Ile1061Phe
ENST00000571763.5:n.336A>T
ENST00000574740.1:n.367A>T
ENST00000576720.1:n.3369A>T
NM_001079846.1:c.4432A>T	NP_001073315.1:p.Ile1478Phe
NM_004380.2:c.4546A>T	NP_004371.2:p.Ile1516Phe
XM_005255124.3:c.4501A>T	XP_005255181.1:p.Ile1501Phe
XM_005255125.3:c.4129A>T	XP_005255182.1:p.Ile1377Phe
XM_006720848.2:c.4285A>T	XP_006720911.1:p.Ile1429Phe
XM_011522380.1:c.4492A>T	XP_011520682.1:p.Ile1498Phe
XM_011522381.1:c.3793A>T	XP_011520683.1:p.Ile1265Phe
XM_005255124.4:c.4501A>T	XP_005255181.1:p.Ile1501Phe
XM_005255125.4:c.4129A>T	XP_005255182.1:p.Ile1377Phe
XM_006720848.3:c.4285A>T	XP_006720911.1:p.Ile1429Phe
XM_011522381.2:c.3793A>T	XP_011520683.1:p.Ile1265Phe
XM_017022944.1:c.4540A>T	XP_016878433.1:p.Ile1514Phe
NM_004380.3:c.4546A>T MANE Select	NP_004371.2:p.Ile1516Phe