Canonical Allele Identifier: CA394571150
Community Standard Title: NM_004380.3(CREBBP):c.3061-1G>T
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3767910C>A , CM000678.2:g.3767910C>A GRCh38
NC_000016.9:g.3817911C>A , CM000678.1:g.3817911C>A GRCh37
NC_000016.8:g.3757912C>A NCBI36
NG_009873.1:g.117211G>T
NG_009873.2:g.117804G>T

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.3061-1G>T MANE Select NP_004371.2:n.3061-1G>T
ENST00000262367.10:c.3061-1G>T MANE Select ENSP00000262367.5:n.3061-1G>T
NM_001079846.1:c.2947-1G>T NP_001073315.1:n.2947-1G>T
NM_004380.2:c.3061-1G>T NP_004371.2:n.3061-1G>T
ENST00000262367.9:c.3061-1G>T ENSP00000262367.5:n.3061-1G>T
ENST00000382070.7:c.2947-1G>T ENSP00000371502.3:n.2947-1G>T
ENST00000570939.2:c.1666-1G>T ENSP00000461002.2:n.1666-1G>T
ENST00000573672.1:n.315-1G>T
XM_005255124.3:c.3016-1G>T XP_005255181.1:n.3016-1G>T
XM_005255124.4:c.3016-1G>T XP_005255181.1:n.3016-1G>T
XM_005255125.3:c.2644-1G>T XP_005255182.1:n.2644-1G>T
XM_005255125.4:c.2644-1G>T XP_005255182.1:n.2644-1G>T
XM_006720848.2:c.3061-1G>T XP_006720911.1:n.3061-1G>T
XM_006720848.3:c.3061-1G>T XP_006720911.1:n.3061-1G>T
XM_011522380.1:c.3007-1G>T XP_011520682.1:n.3007-1G>T
XM_011522381.1:c.2308-1G>T XP_011520683.1:n.2308-1G>T
XM_011522381.2:c.2308-1G>T XP_011520683.1:n.2308-1G>T
XM_011522382.1:c.3061-1G>T XP_011520684.1:n.3061-1G>T
XM_011522382.3:c.3061-1G>T XP_011520684.1:n.3061-1G>T
XM_017022944.1:c.3055-1G>T XP_016878433.1:n.3055-1G>T