Canonical Allele Identifier: CA2202950920
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3770852C= , CM000678.2:g.3770852C= GRCh38
NC_000016.9:g.3820853C= , CM000678.1:g.3820853C= GRCh37
NC_000016.8:g.3760854C= NCBI36
NG_009873.1:g.114269G=
NG_009873.2:g.114862G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2598G= MANE Select ENSP00000262367.5:p.Met866=
ENST00000262367.9:c.2598G= ENSP00000262367.5:p.Met866=
ENST00000382070.7:c.2484G= ENSP00000371502.3:p.Met828=
ENST00000570939.2:c.1203G= ENSP00000461002.2:p.Met401=
NM_001079846.1:c.2484G= NP_001073315.1:p.Met828=
NM_004380.2:c.2598G= NP_004371.2:p.Met866=
XM_005255124.3:c.2553G= XP_005255181.1:p.Met851=
XM_005255125.3:c.2464-1499G= XP_005255182.1:n.2464-1499G=
XM_006720848.2:c.2598G= XP_006720911.1:p.Met866=
XM_011522380.1:c.2544G= XP_011520682.1:p.Met848=
XM_011522381.1:c.1845G= XP_011520683.1:p.Met615=
XM_011522382.1:c.2598G= XP_011520684.1:p.Met866=
XM_005255124.4:c.2553G= XP_005255181.1:p.Met851=
XM_005255125.4:c.2464-1499G= XP_005255182.1:n.2464-1499G=
XM_006720848.3:c.2598G= XP_006720911.1:p.Met866=
XM_011522381.2:c.1845G= XP_011520683.1:p.Met615=
XM_011522382.3:c.2598G= XP_011520684.1:p.Met866=
XM_017022944.1:c.2592G= XP_016878433.1:p.Met864=
NM_004380.3:c.2598G= MANE Select NP_004371.2:p.Met866=