Canonical Allele Identifier: CA2202943259
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3757894T= , CM000678.2:g.3757894T= GRCh38
NC_000016.9:g.3807895T= , CM000678.1:g.3807895T= GRCh37
NC_000016.8:g.3747896T= NCBI36
NG_009873.1:g.127227A=
NG_009873.2:g.127820A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3524A= MANE Select ENSP00000262367.5:p.Tyr1175=
ENST00000262367.9:c.3524A= ENSP00000262367.5:p.Tyr1175=
ENST00000382070.7:c.3410A= ENSP00000371502.3:p.Tyr1137=
ENST00000570939.2:c.2129A= ENSP00000461002.2:p.Tyr710=
NM_001079846.1:c.3410A= NP_001073315.1:p.Tyr1137=
NM_004380.2:c.3524A= NP_004371.2:p.Tyr1175=
XM_005255124.3:c.3479A= XP_005255181.1:p.Tyr1160=
XM_005255125.3:c.3107A= XP_005255182.1:p.Tyr1036=
XM_006720848.2:c.3524A= XP_006720911.1:p.Tyr1175=
XM_011522380.1:c.3470A= XP_011520682.1:p.Tyr1157=
XM_011522381.1:c.2771A= XP_011520683.1:p.Tyr924=
XM_011522382.1:c.3524A= XP_011520684.1:p.Tyr1175=
XM_005255124.4:c.3479A= XP_005255181.1:p.Tyr1160=
XM_005255125.4:c.3107A= XP_005255182.1:p.Tyr1036=
XM_006720848.3:c.3524A= XP_006720911.1:p.Tyr1175=
XM_011522381.2:c.2771A= XP_011520683.1:p.Tyr924=
XM_011522382.3:c.3524A= XP_011520684.1:p.Tyr1175=
XM_017022944.1:c.3518A= XP_016878433.1:p.Tyr1173=
NM_004380.3:c.3524A= MANE Select NP_004371.2:p.Tyr1175=