Canonical Allele Identifier: CA2202958525

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3777913_3777914delinsCA , CM000678.2:g.3777913_3777914delinsCA	GRCh38
NC_000016.9:g.3827914_3827915delinsCA , CM000678.1:g.3827914_3827915delinsCA	GRCh37
NC_000016.8:g.3767915_3767916delinsCA	NCBI36
NG_009873.1:g.107207_107208delinsTG
NG_009873.2:g.107800_107801delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2113+97_2113+98delinsTG MANE Select	ENSP00000262367.5:n.2113+97_2113+98delinsTG
ENST00000262367.9:c.2113+97_2113+98delinsTG	ENSP00000262367.5:n.2113+97_2113+98delinsTG
ENST00000382070.7:c.1999+97_1999+98delinsTG	ENSP00000371502.3:n.1999+97_1999+98delinsTG
ENST00000570939.2:c.718+97_718+98delinsTG	ENSP00000461002.2:n.718+97_718+98delinsTG
ENST00000571826.5:c.162+97_162+98delinsTG
ENST00000572134.1:c.426+97_426+98delinsTG
NM_001079846.1:c.1999+97_1999+98delinsTG	NP_001073315.1:n.1999+97_1999+98delinsTG
NM_004380.2:c.2113+97_2113+98delinsTG	NP_004371.2:n.2113+97_2113+98delinsTG
XM_005255124.3:c.2113+97_2113+98delinsTG	XP_005255181.1:n.2113+97_2113+98delinsTG
XM_005255125.3:c.2113+97_2113+98delinsTG	XP_005255182.1:n.2113+97_2113+98delinsTG
XM_006720848.2:c.2113+97_2113+98delinsTG	XP_006720911.1:n.2113+97_2113+98delinsTG
XM_011522380.1:c.2059+97_2059+98delinsTG	XP_011520682.1:n.2059+97_2059+98delinsTG
XM_011522381.1:c.1360+97_1360+98delinsTG	XP_011520683.1:n.1360+97_1360+98delinsTG
XM_011522382.1:c.2113+97_2113+98delinsTG	XP_011520684.1:n.2113+97_2113+98delinsTG
XM_005255124.4:c.2113+97_2113+98delinsTG	XP_005255181.1:n.2113+97_2113+98delinsTG
XM_005255125.4:c.2113+97_2113+98delinsTG	XP_005255182.1:n.2113+97_2113+98delinsTG
XM_006720848.3:c.2113+97_2113+98delinsTG	XP_006720911.1:n.2113+97_2113+98delinsTG
XM_011522381.2:c.1360+97_1360+98delinsTG	XP_011520683.1:n.1360+97_1360+98delinsTG
XM_011522382.3:c.2113+97_2113+98delinsTG	XP_011520684.1:n.2113+97_2113+98delinsTG
XM_017022944.1:c.2113+97_2113+98delinsTG	XP_016878433.1:n.2113+97_2113+98delinsTG
NM_004380.3:c.2113+97_2113+98delinsTG MANE Select	NP_004371.2:n.2113+97_2113+98delinsTG