Canonical Allele Identifier: CA394564004
Community Standard Title: NM_004380.3(CREBBP):c.4417G>A (p.Ala1473Thr)
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736793C>T , CM000678.2:g.3736793C>T GRCh38
NC_000016.9:g.3786794C>T , CM000678.1:g.3786794C>T GRCh37
NC_000016.8:g.3726795C>T NCBI36
NG_009873.1:g.148328G>A
NG_009873.2:g.148921G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.4417G>A MANE Select NP_004371.2:p.Ala1473Thr
ENST00000262367.10:c.4417G>A MANE Select ENSP00000262367.5:p.Ala1473Thr
NM_001079846.1:c.4303G>A NP_001073315.1:p.Ala1435Thr
NM_004380.2:c.4417G>A NP_004371.2:p.Ala1473Thr
ENST00000262367.9:c.4417G>A ENSP00000262367.5:p.Ala1473Thr
ENST00000382070.7:c.4303G>A ENSP00000371502.3:p.Ala1435Thr
ENST00000570939.2:c.3052G>A ENSP00000461002.2:p.Ala1018Thr
ENST00000571763.5:n.207G>A
ENST00000574740.1:n.238G>A
ENST00000576720.1:n.3240G>A
XM_005255124.3:c.4372G>A XP_005255181.1:p.Ala1458Thr
XM_005255124.4:c.4372G>A XP_005255181.1:p.Ala1458Thr
XM_005255125.3:c.4000G>A XP_005255182.1:p.Ala1334Thr
XM_005255125.4:c.4000G>A XP_005255182.1:p.Ala1334Thr
XM_006720848.2:c.4156G>A XP_006720911.1:p.Ala1386Thr
XM_006720848.3:c.4156G>A XP_006720911.1:p.Ala1386Thr
XM_011522380.1:c.4363G>A XP_011520682.1:p.Ala1455Thr
XM_011522381.1:c.3664G>A XP_011520683.1:p.Ala1222Thr
XM_011522381.2:c.3664G>A XP_011520683.1:p.Ala1222Thr
XM_017022944.1:c.4411G>A XP_016878433.1:p.Ala1471Thr