Canonical Allele Identifier: CA394563618
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736714A>C , CM000678.2:g.3736714A>C GRCh38
NC_000016.9:g.3786715A>C , CM000678.1:g.3786715A>C GRCh37
NC_000016.8:g.3726716A>C NCBI36
NG_009873.1:g.148407T>G
NG_009873.2:g.149000T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4496T>G MANE Select ENSP00000262367.5:p.Leu1499Arg
ENST00000262367.9:c.4496T>G ENSP00000262367.5:p.Leu1499Arg
ENST00000382070.7:c.4382T>G ENSP00000371502.3:p.Leu1461Arg
ENST00000570939.2:c.3131T>G ENSP00000461002.2:p.Leu1044Arg
ENST00000571763.5:n.286T>G
ENST00000574740.1:n.317T>G
ENST00000576720.1:n.3319T>G
NM_001079846.1:c.4382T>G NP_001073315.1:p.Leu1461Arg
NM_004380.2:c.4496T>G NP_004371.2:p.Leu1499Arg
XM_005255124.3:c.4451T>G XP_005255181.1:p.Leu1484Arg
XM_005255125.3:c.4079T>G XP_005255182.1:p.Leu1360Arg
XM_006720848.2:c.4235T>G XP_006720911.1:p.Leu1412Arg
XM_011522380.1:c.4442T>G XP_011520682.1:p.Leu1481Arg
XM_011522381.1:c.3743T>G XP_011520683.1:p.Leu1248Arg
XM_005255124.4:c.4451T>G XP_005255181.1:p.Leu1484Arg
XM_005255125.4:c.4079T>G XP_005255182.1:p.Leu1360Arg
XM_006720848.3:c.4235T>G XP_006720911.1:p.Leu1412Arg
XM_011522381.2:c.3743T>G XP_011520683.1:p.Leu1248Arg
XM_017022944.1:c.4490T>G XP_016878433.1:p.Leu1497Arg
NM_004380.3:c.4496T>G MANE Select NP_004371.2:p.Leu1499Arg