Canonical Allele Identifier: CA394563679
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2052070989

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736726T>A , CM000678.2:g.3736726T>A GRCh38
NC_000016.9:g.3786727T>A , CM000678.1:g.3786727T>A GRCh37
NC_000016.8:g.3726728T>A NCBI36
NG_009873.1:g.148395A>T
NG_009873.2:g.148988A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4484A>T MANE Select ENSP00000262367.5:p.Lys1495Met
ENST00000262367.9:c.4484A>T ENSP00000262367.5:p.Lys1495Met
ENST00000382070.7:c.4370A>T ENSP00000371502.3:p.Lys1457Met
ENST00000570939.2:c.3119A>T ENSP00000461002.2:p.Lys1040Met
ENST00000571763.5:n.274A>T
ENST00000574740.1:n.305A>T
ENST00000576720.1:n.3307A>T
NM_001079846.1:c.4370A>T NP_001073315.1:p.Lys1457Met
NM_004380.2:c.4484A>T NP_004371.2:p.Lys1495Met
XM_005255124.3:c.4439A>T XP_005255181.1:p.Lys1480Met
XM_005255125.3:c.4067A>T XP_005255182.1:p.Lys1356Met
XM_006720848.2:c.4223A>T XP_006720911.1:p.Lys1408Met
XM_011522380.1:c.4430A>T XP_011520682.1:p.Lys1477Met
XM_011522381.1:c.3731A>T XP_011520683.1:p.Lys1244Met
XM_005255124.4:c.4439A>T XP_005255181.1:p.Lys1480Met
XM_005255125.4:c.4067A>T XP_005255182.1:p.Lys1356Met
XM_006720848.3:c.4223A>T XP_006720911.1:p.Lys1408Met
XM_011522381.2:c.3731A>T XP_011520683.1:p.Lys1244Met
XM_017022944.1:c.4478A>T XP_016878433.1:p.Lys1493Met
NM_004380.3:c.4484A>T MANE Select NP_004371.2:p.Lys1495Met