Canonical Allele Identifier: CA394563348

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3786667A>G (hg19) ; chr16:g.3736666A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736666A>G , CM000678.2:g.3736666A>G	GRCh38
NC_000016.9:g.3786667A>G , CM000678.1:g.3786667A>G	GRCh37
NC_000016.8:g.3726668A>G	NCBI36
NG_009873.1:g.148455T>C
NG_009873.2:g.149048T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4544T>C MANE Select	ENSP00000262367.5:p.Ile1515Thr
ENST00000262367.9:c.4544T>C	ENSP00000262367.5:p.Ile1515Thr
ENST00000382070.7:c.4430T>C	ENSP00000371502.3:p.Ile1477Thr
ENST00000570939.2:c.3179T>C	ENSP00000461002.2:p.Ile1060Thr
ENST00000571763.5:n.334T>C
ENST00000574740.1:n.365T>C
ENST00000576720.1:n.3367T>C
NM_001079846.1:c.4430T>C	NP_001073315.1:p.Ile1477Thr
NM_004380.2:c.4544T>C	NP_004371.2:p.Ile1515Thr
XM_005255124.3:c.4499T>C	XP_005255181.1:p.Ile1500Thr
XM_005255125.3:c.4127T>C	XP_005255182.1:p.Ile1376Thr
XM_006720848.2:c.4283T>C	XP_006720911.1:p.Ile1428Thr
XM_011522380.1:c.4490T>C	XP_011520682.1:p.Ile1497Thr
XM_011522381.1:c.3791T>C	XP_011520683.1:p.Ile1264Thr
XM_005255124.4:c.4499T>C	XP_005255181.1:p.Ile1500Thr
XM_005255125.4:c.4127T>C	XP_005255182.1:p.Ile1376Thr
XM_006720848.3:c.4283T>C	XP_006720911.1:p.Ile1428Thr
XM_011522381.2:c.3791T>C	XP_011520683.1:p.Ile1264Thr
XM_017022944.1:c.4538T>C	XP_016878433.1:p.Ile1513Thr
NM_004380.3:c.4544T>C MANE Select	NP_004371.2:p.Ile1515Thr