Canonical Allele Identifier: CA2631426695
Gene: CREBBP HGNC NCBI

Linked Data

gnomAD v4: 16-3777554-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3777554G>A , CM000678.2:g.3777554G>A GRCh38
NC_000016.9:g.3827555G>A , CM000678.1:g.3827555G>A GRCh37
NC_000016.8:g.3767556G>A NCBI36
NG_009873.1:g.107567C>T
NG_009873.2:g.108160C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2158+59C>T MANE Select ENSP00000262367.5:n.2158+59C>T
ENST00000262367.9:c.2158+59C>T ENSP00000262367.5:n.2158+59C>T
ENST00000382070.7:c.2044+59C>T ENSP00000371502.3:n.2044+59C>T
ENST00000570939.2:c.763+59C>T ENSP00000461002.2:n.763+59C>T
ENST00000571826.5:c.207+59C>T
ENST00000572134.1:c.426+457C>T
NM_001079846.1:c.2044+59C>T NP_001073315.1:n.2044+59C>T
NM_004380.2:c.2158+59C>T NP_004371.2:n.2158+59C>T
XM_005255124.3:c.2113+457C>T XP_005255181.1:n.2113+457C>T
XM_005255125.3:c.2158+59C>T XP_005255182.1:n.2158+59C>T
XM_006720848.2:c.2158+59C>T XP_006720911.1:n.2158+59C>T
XM_011522380.1:c.2104+59C>T XP_011520682.1:n.2104+59C>T
XM_011522381.1:c.1405+59C>T XP_011520683.1:n.1405+59C>T
XM_011522382.1:c.2158+59C>T XP_011520684.1:n.2158+59C>T
XM_005255124.4:c.2113+457C>T XP_005255181.1:n.2113+457C>T
XM_005255125.4:c.2158+59C>T XP_005255182.1:n.2158+59C>T
XM_006720848.3:c.2158+59C>T XP_006720911.1:n.2158+59C>T
XM_011522381.2:c.1405+59C>T XP_011520683.1:n.1405+59C>T
XM_011522382.3:c.2158+59C>T XP_011520684.1:n.2158+59C>T
XM_017022944.1:c.2158+59C>T XP_016878433.1:n.2158+59C>T
NM_004380.3:c.2158+59C>T MANE Select NP_004371.2:n.2158+59C>T