Canonical Allele Identifier: CA394556244
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs1431269013

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729573A>G , CM000678.2:g.3729573A>G GRCh38
NC_000016.9:g.3779574A>G , CM000678.1:g.3779574A>G GRCh37
NC_000016.8:g.3719575A>G NCBI36
NG_009873.1:g.155548T>C
NG_009873.2:g.156141T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5474T>C MANE Select ENSP00000262367.5:p.Leu1825Pro
ENST00000262367.9:c.5474T>C ENSP00000262367.5:p.Leu1825Pro
ENST00000382070.7:c.5360T>C ENSP00000371502.3:p.Leu1787Pro
NM_001079846.1:c.5360T>C NP_001073315.1:p.Leu1787Pro
NM_004380.2:c.5474T>C NP_004371.2:p.Leu1825Pro
XM_005255124.3:c.5429T>C XP_005255181.1:p.Leu1810Pro
XM_005255125.3:c.5057T>C XP_005255182.1:p.Leu1686Pro
XM_006720848.2:c.5213T>C XP_006720911.1:p.Leu1738Pro
XM_011522380.1:c.5420T>C XP_011520682.1:p.Leu1807Pro
XM_011522381.1:c.4721T>C XP_011520683.1:p.Leu1574Pro
XM_005255124.4:c.5429T>C XP_005255181.1:p.Leu1810Pro
XM_005255125.4:c.5057T>C XP_005255182.1:p.Leu1686Pro
XM_006720848.3:c.5213T>C XP_006720911.1:p.Leu1738Pro
XM_011522381.2:c.4721T>C XP_011520683.1:p.Leu1574Pro
XM_017022944.1:c.5468T>C XP_016878433.1:p.Leu1823Pro
NM_004380.3:c.5474T>C MANE Select NP_004371.2:p.Leu1825Pro