Canonical Allele Identifier: CA277030

Gene: CREBBP

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3757982G>A , CM000678.2:g.3757982G>A	GRCh38
NC_000016.9:g.3807983G>A , CM000678.1:g.3807983G>A	GRCh37
NC_000016.8:g.3747984G>A	NCBI36
NG_009873.1:g.127139C>T
NG_009873.2:g.127732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.3436C>T MANE Select	ENSP00000262367.5:p.Gln1146Ter
ENST00000262367.9:c.3436C>T	ENSP00000262367.5:p.Gln1146Ter
ENST00000382070.7:c.3322C>T	ENSP00000371502.3:p.Gln1108Ter
ENST00000570939.2:c.2041C>T	ENSP00000461002.2:p.Gln681Ter
NM_001079846.1:c.3322C>T	NP_001073315.1:p.Gln1108Ter
NM_004380.2:c.3436C>T	NP_004371.2:p.Gln1146Ter
XM_005255124.3:c.3391C>T	XP_005255181.1:p.Gln1131Ter
XM_005255125.3:c.3019C>T	XP_005255182.1:p.Gln1007Ter
XM_006720848.2:c.3436C>T	XP_006720911.1:p.Gln1146Ter
XM_011522380.1:c.3382C>T	XP_011520682.1:p.Gln1128Ter
XM_011522381.1:c.2683C>T	XP_011520683.1:p.Gln895Ter
XM_011522382.1:c.3436C>T	XP_011520684.1:p.Gln1146Ter
XM_005255124.4:c.3391C>T	XP_005255181.1:p.Gln1131Ter
XM_005255125.4:c.3019C>T	XP_005255182.1:p.Gln1007Ter
XM_006720848.3:c.3436C>T	XP_006720911.1:p.Gln1146Ter
XM_011522381.2:c.2683C>T	XP_011520683.1:p.Gln895Ter
XM_011522382.3:c.3436C>T	XP_011520684.1:p.Gln1146Ter
XM_017022944.1:c.3430C>T	XP_016878433.1:p.Gln1144Ter
NM_004380.3:c.3436C>T MANE Select	NP_004371.2:p.Gln1146Ter