Canonical Allele Identifier: CA2202930878
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3746058_3746060delinsTAA , CM000678.2:g.3746058_3746060delinsTAA GRCh38
NC_000016.9:g.3796059_3796061delinsTAA , CM000678.1:g.3796059_3796061delinsTAA GRCh37
NC_000016.8:g.3736060_3736062delinsTAA NCBI36
NG_009873.1:g.139061_139063delinsTTA
NG_009873.2:g.139654_139656delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3837-706_3837-704delinsTTA MANE Select ENSP00000262367.5:n.3837-706_3837-704deli...
ENST00000638158.1:n.58-465_58-463delinsTTA
ENST00000262367.9:c.3837-706_3837-704delinsTTA ENSP00000262367.5:n.3837-706_3837-704deli...
ENST00000382070.7:c.3723-706_3723-704delinsTTA ENSP00000371502.3:n.3723-706_3723-704deli...
ENST00000570939.2:c.2472-706_2472-704delinsTTA ENSP00000461002.2:n.2472-706_2472-704deli...
ENST00000573517.6:c.143-706_143-704delinsTTA
NM_001079846.1:c.3723-706_3723-704delinsTTA NP_001073315.1:n.3723-706_3723-704delinsT...
NM_004380.2:c.3837-706_3837-704delinsTTA NP_004371.2:n.3837-706_3837-704delinsTTA
XM_005255124.3:c.3792-706_3792-704delinsTTA XP_005255181.1:n.3792-706_3792-704delinsT...
XM_005255125.3:c.3420-706_3420-704delinsTTA XP_005255182.1:n.3420-706_3420-704delinsT...
XM_006720848.2:c.3837-706_3837-704delinsTTA XP_006720911.1:n.3837-706_3837-704delinsT...
XM_011522380.1:c.3783-706_3783-704delinsTTA XP_011520682.1:n.3783-706_3783-704delinsT...
XM_011522381.1:c.3084-706_3084-704delinsTTA XP_011520683.1:n.3084-706_3084-704delinsT...
XM_011522382.1:c.3837-465_3837-463delinsTTA XP_011520684.1:n.3837-465_3837-463delinsT...
XM_005255124.4:c.3792-706_3792-704delinsTTA XP_005255181.1:n.3792-706_3792-704delinsT...
XM_005255125.4:c.3420-706_3420-704delinsTTA XP_005255182.1:n.3420-706_3420-704delinsT...
XM_006720848.3:c.3837-706_3837-704delinsTTA XP_006720911.1:n.3837-706_3837-704delinsT...
XM_011522381.2:c.3084-706_3084-704delinsTTA XP_011520683.1:n.3084-706_3084-704delinsT...
XM_011522382.3:c.3837-465_3837-463delinsTTA XP_011520684.1:n.3837-465_3837-463delinsT...
XM_017022944.1:c.3831-706_3831-704delinsTTA XP_016878433.1:n.3831-706_3831-704delinsT...
NM_004380.3:c.3837-706_3837-704delinsTTA MANE Select NP_004371.2:n.3837-706_3837-704delinsTTA