Canonical Allele Identifier: CA394549562
Community Standard Title: NM_004380.3(CREBBP):c.3060+1G>T
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3769173C>A , CM000678.2:g.3769173C>A GRCh38
NC_000016.9:g.3819174C>A , CM000678.1:g.3819174C>A GRCh37
NC_000016.8:g.3759175C>A NCBI36
NG_009873.1:g.115948G>T
NG_009873.2:g.116541G>T

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.3060+1G>T MANE Select NP_004371.2:n.3060+1G>T
ENST00000262367.10:c.3060+1G>T MANE Select ENSP00000262367.5:n.3060+1G>T
NM_001079846.1:c.2946+1G>T NP_001073315.1:n.2946+1G>T
NM_004380.2:c.3060+1G>T NP_004371.2:n.3060+1G>T
ENST00000262367.9:c.3060+1G>T ENSP00000262367.5:n.3060+1G>T
ENST00000382070.7:c.2946+1G>T ENSP00000371502.3:n.2946+1G>T
ENST00000570939.2:c.1665+1G>T ENSP00000461002.2:n.1665+1G>T
ENST00000573672.1:n.314+1G>T
XM_005255124.3:c.3015+1G>T XP_005255181.1:n.3015+1G>T
XM_005255124.4:c.3015+1G>T XP_005255181.1:n.3015+1G>T
XM_005255125.3:c.2643+1G>T XP_005255182.1:n.2643+1G>T
XM_005255125.4:c.2643+1G>T XP_005255182.1:n.2643+1G>T
XM_006720848.2:c.3060+1G>T XP_006720911.1:n.3060+1G>T
XM_006720848.3:c.3060+1G>T XP_006720911.1:n.3060+1G>T
XM_011522380.1:c.3006+1G>T XP_011520682.1:n.3006+1G>T
XM_011522381.1:c.2307+1G>T XP_011520683.1:n.2307+1G>T
XM_011522381.2:c.2307+1G>T XP_011520683.1:n.2307+1G>T
XM_011522382.1:c.3060+1G>T XP_011520684.1:n.3060+1G>T
XM_011522382.3:c.3060+1G>T XP_011520684.1:n.3060+1G>T
XM_017022944.1:c.3054+1G>T XP_016878433.1:n.3054+1G>T