Canonical Allele Identifier: CA394563122
Community Standard Title: NM_004380.3(CREBBP):c.4561-1G>A
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736204C>T , CM000678.2:g.3736204C>T GRCh38
NC_000016.9:g.3786205C>T , CM000678.1:g.3786205C>T GRCh37
NC_000016.8:g.3726206C>T NCBI36
NG_009873.1:g.148917G>A
NG_009873.2:g.149510G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.4561-1G>A MANE Select NP_004371.2:n.4561-1G>A
ENST00000262367.10:c.4561-1G>A MANE Select ENSP00000262367.5:n.4561-1G>A
NM_001079846.1:c.4447-1G>A NP_001073315.1:n.4447-1G>A
NM_004380.2:c.4561-1G>A NP_004371.2:n.4561-1G>A
ENST00000262367.9:c.4561-1G>A ENSP00000262367.5:n.4561-1G>A
ENST00000382070.7:c.4447-1G>A ENSP00000371502.3:n.4447-1G>A
ENST00000570939.2:c.3196-1G>A ENSP00000461002.2:n.3196-1G>A
ENST00000571763.5:n.351-1G>A
ENST00000576720.1:n.3384-1G>A
XM_005255124.3:c.4516-1G>A XP_005255181.1:n.4516-1G>A
XM_005255124.4:c.4516-1G>A XP_005255181.1:n.4516-1G>A
XM_005255125.3:c.4144-1G>A XP_005255182.1:n.4144-1G>A
XM_005255125.4:c.4144-1G>A XP_005255182.1:n.4144-1G>A
XM_006720848.2:c.4300-1G>A XP_006720911.1:n.4300-1G>A
XM_006720848.3:c.4300-1G>A XP_006720911.1:n.4300-1G>A
XM_011522380.1:c.4507-1G>A XP_011520682.1:n.4507-1G>A
XM_011522381.1:c.3808-1G>A XP_011520683.1:n.3808-1G>A
XM_011522381.2:c.3808-1G>A XP_011520683.1:n.3808-1G>A
XM_017022944.1:c.4555-1G>A XP_016878433.1:n.4555-1G>A