Canonical Allele Identifier: CA7870702
Community Standard Title: NM_004380.3(CREBBP):c.288G>A (p.Gln96=)
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3850807C>T , CM000678.2:g.3850807C>T GRCh38
NC_000016.9:g.3900808C>T , CM000678.1:g.3900808C>T GRCh37
NC_000016.8:g.3840809C>T NCBI36
NG_009873.1:g.34314G>A
NG_009873.2:g.34907G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.288G>A MANE Select NP_004371.2:p.Gln96=
ENST00000262367.10:c.288G>A MANE Select ENSP00000262367.5:p.Gln96=
NM_001079846.1:c.288G>A NP_001073315.1:p.Gln96=
NM_004380.2:c.288G>A NP_004371.2:p.Gln96=
ENST00000262367.9:c.288G>A ENSP00000262367.5:p.Gln96=
ENST00000382070.7:c.288G>A ENSP00000371502.3:p.Gln96=
XM_005255124.3:c.288G>A XP_005255181.1:p.Gln96=
XM_005255124.4:c.288G>A XP_005255181.1:p.Gln96=
XM_005255125.3:c.288G>A XP_005255182.1:p.Gln96=
XM_005255125.4:c.288G>A XP_005255182.1:p.Gln96=
XM_006720848.2:c.288G>A XP_006720911.1:p.Gln96=
XM_006720848.3:c.288G>A XP_006720911.1:p.Gln96=
XM_011522380.1:c.234G>A XP_011520682.1:p.Gln78=
XM_011522382.1:c.288G>A XP_011520684.1:p.Gln96=
XM_011522382.3:c.288G>A XP_011520684.1:p.Gln96=
XM_017022944.1:c.288G>A XP_016878433.1:p.Gln96=