Canonical Allele Identifier: CA493279231
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151329349
MyVariant Identifiers: chr16:g.3786692G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736691G>A , CM000678.2:g.3736691G>A GRCh38
NC_000016.9:g.3786692G>A , CM000678.1:g.3786692G>A GRCh37
NC_000016.8:g.3726693G>A NCBI36
NG_009873.1:g.148430C>T
NG_009873.2:g.149023C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4519C>T MANE Select ENSP00000262367.5:p.Leu1507=
ENST00000262367.9:c.4519C>T ENSP00000262367.5:p.Leu1507=
ENST00000382070.7:c.4405C>T ENSP00000371502.3:p.Leu1469=
ENST00000570939.2:c.3154C>T ENSP00000461002.2:p.Leu1052=
ENST00000571763.5:n.309C>T
ENST00000574740.1:n.340C>T
ENST00000576720.1:n.3342C>T
NM_001079846.1:c.4405C>T NP_001073315.1:p.Leu1469=
NM_004380.2:c.4519C>T NP_004371.2:p.Leu1507=
XM_005255124.3:c.4474C>T XP_005255181.1:p.Leu1492=
XM_005255125.3:c.4102C>T XP_005255182.1:p.Leu1368=
XM_006720848.2:c.4258C>T XP_006720911.1:p.Leu1420=
XM_011522380.1:c.4465C>T XP_011520682.1:p.Leu1489=
XM_011522381.1:c.3766C>T XP_011520683.1:p.Leu1256=
XM_005255124.4:c.4474C>T XP_005255181.1:p.Leu1492=
XM_005255125.4:c.4102C>T XP_005255182.1:p.Leu1368=
XM_006720848.3:c.4258C>T XP_006720911.1:p.Leu1420=
XM_011522381.2:c.3766C>T XP_011520683.1:p.Leu1256=
XM_017022944.1:c.4513C>T XP_016878433.1:p.Leu1505=
NM_004380.3:c.4519C>T MANE Select NP_004371.2:p.Leu1507=