Canonical Allele Identifier: CA2202958477

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3777871_3777873delinsTCA , CM000678.2:g.3777871_3777873delinsTCA	GRCh38
NC_000016.9:g.3827872_3827874delinsTCA , CM000678.1:g.3827872_3827874delinsTCA	GRCh37
NC_000016.8:g.3767873_3767875delinsTCA	NCBI36
NG_009873.1:g.107248_107250delinsTGA
NG_009873.2:g.107841_107843delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2113+138_2113+140delinsTGA MANE Select	ENSP00000262367.5:n.2113+138_2113+140delinsTGA
ENST00000262367.9:c.2113+138_2113+140delinsTGA	ENSP00000262367.5:n.2113+138_2113+140delinsTGA
ENST00000382070.7:c.1999+138_1999+140delinsTGA	ENSP00000371502.3:n.1999+138_1999+140delinsTGA
ENST00000570939.2:c.718+138_718+140delinsTGA	ENSP00000461002.2:n.718+138_718+140delinsTGA
ENST00000571826.5:c.162+138_162+140delinsTGA
ENST00000572134.1:c.426+138_426+140delinsTGA
NM_001079846.1:c.1999+138_1999+140delinsTGA	NP_001073315.1:n.1999+138_1999+140delinsTGA
NM_004380.2:c.2113+138_2113+140delinsTGA	NP_004371.2:n.2113+138_2113+140delinsTGA
XM_005255124.3:c.2113+138_2113+140delinsTGA	XP_005255181.1:n.2113+138_2113+140delinsTGA
XM_005255125.3:c.2113+138_2113+140delinsTGA	XP_005255182.1:n.2113+138_2113+140delinsTGA
XM_006720848.2:c.2113+138_2113+140delinsTGA	XP_006720911.1:n.2113+138_2113+140delinsTGA
XM_011522380.1:c.2059+138_2059+140delinsTGA	XP_011520682.1:n.2059+138_2059+140delinsTGA
XM_011522381.1:c.1360+138_1360+140delinsTGA	XP_011520683.1:n.1360+138_1360+140delinsTGA
XM_011522382.1:c.2113+138_2113+140delinsTGA	XP_011520684.1:n.2113+138_2113+140delinsTGA
XM_005255124.4:c.2113+138_2113+140delinsTGA	XP_005255181.1:n.2113+138_2113+140delinsTGA
XM_005255125.4:c.2113+138_2113+140delinsTGA	XP_005255182.1:n.2113+138_2113+140delinsTGA
XM_006720848.3:c.2113+138_2113+140delinsTGA	XP_006720911.1:n.2113+138_2113+140delinsTGA
XM_011522381.2:c.1360+138_1360+140delinsTGA	XP_011520683.1:n.1360+138_1360+140delinsTGA
XM_011522382.3:c.2113+138_2113+140delinsTGA	XP_011520684.1:n.2113+138_2113+140delinsTGA
XM_017022944.1:c.2113+138_2113+140delinsTGA	XP_016878433.1:n.2113+138_2113+140delinsTGA
NM_004380.3:c.2113+138_2113+140delinsTGA MANE Select	NP_004371.2:n.2113+138_2113+140delinsTGA