Canonical Allele Identifier: CA1601985754

Gene: CPEB4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173932680_173932682delinsAAT , CM000667.2:g.173932680_173932682delinsAAT	GRCh38
NC_000005.9:g.173359683_173359685delinsAAT , CM000667.1:g.173359683_173359685delinsAAT	GRCh37
NC_000005.8:g.173292289_173292291delinsAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265085.10:c.1258+180_1258+182delinsAAT MANE Select	ENSP00000265085.5:n.1258+180_1258+182delinsAAT
ENST00000657000.1:c.-20-12287_-20-12285delinsAAT	ENSP00000499433.1:n.-20-12287_-20-12285delinsAAT
ENST00000659882.1:c.51+180_51+182delinsAAT
ENST00000265085.9:c.1258+180_1258+182delinsAAT	ENSP00000265085.5:n.1258+180_1258+182delinsAAT
ENST00000334035.9:c.1208-10346_1208-10344delinsAAT	ENSP00000334533.5:n.1208-10346_1208-10344delinsAAT
ENST00000517880.1:c.62-12287_62-12285delinsAAT	ENSP00000427990.1:n.62-12287_62-12285delinsAAT
ENST00000519152.5:c.315+180_315+182delinsAAT
ENST00000519467.1:n.40-10346_40-10344delinsAAT
ENST00000519835.5:c.1208-12287_1208-12285delinsAAT	ENSP00000429048.1:n.1208-12287_1208-12285delinsAAT
ENST00000520867.5:c.1208-12287_1208-12285delinsAAT	ENSP00000429092.1:n.1208-12287_1208-12285delinsAAT
ENST00000522336.5:c.112+180_112+182delinsAAT	ENSP00000430345.1:n.112+180_112+182delinsAAT
NM_001308189.1:c.1208-10346_1208-10344delinsAAT	NP_001295118.1:n.1208-10346_1208-10344delinsAAT
NM_001308191.1:c.1208-12287_1208-12285delinsAAT	NP_001295120.1:n.1208-12287_1208-12285delinsAAT
NM_001308192.1:c.112+180_112+182delinsAAT	NP_001295121.1:n.112+180_112+182delinsAAT
NM_001308193.1:c.62-12287_62-12285delinsAAT	NP_001295122.1:n.62-12287_62-12285delinsAAT
NM_030627.2:c.1258+180_1258+182delinsAAT	NP_085130.2:n.1258+180_1258+182delinsAAT
NM_030627.3:c.1258+180_1258+182delinsAAT	NP_085130.2:n.1258+180_1258+182delinsAAT
XM_005265994.1:c.1258+180_1258+182delinsAAT	XP_005266051.1:n.1258+180_1258+182delinsAAT
XM_011534660.1:c.1258+180_1258+182delinsAAT	XP_011532962.1:n.1258+180_1258+182delinsAAT
XM_011534661.1:c.1208-10204_1208-10202delinsAAT	XP_011532963.1:n.1208-10204_1208-10202delinsAAT
XM_011534660.2:c.1258+180_1258+182delinsAAT	XP_011532962.1:n.1258+180_1258+182delinsAAT
XM_011534661.2:c.1208-10204_1208-10202delinsAAT	XP_011532963.1:n.1208-10204_1208-10202delinsAAT
NM_030627.4:c.1258+180_1258+182delinsAAT MANE Select	NP_085130.2:n.1258+180_1258+182delinsAAT
NM_001308189.2:c.1208-10346_1208-10344delinsAAT	NP_001295118.1:n.1208-10346_1208-10344delinsAAT
NM_001308191.2:c.1208-12287_1208-12285delinsAAT	NP_001295120.1:n.1208-12287_1208-12285delinsAAT
NM_001308192.2:c.112+180_112+182delinsAAT	NP_001295121.1:n.112+180_112+182delinsAAT
NM_001308193.2:c.62-12287_62-12285delinsAAT	NP_001295122.1:n.62-12287_62-12285delinsAAT