Canonical Allele Identifier: CA1601985594

Gene: CPEB4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173932541_173932542delinsTG , CM000667.2:g.173932541_173932542delinsTG	GRCh38
NC_000005.9:g.173359544_173359545delinsTG , CM000667.1:g.173359544_173359545delinsTG	GRCh37
NC_000005.8:g.173292150_173292151delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265085.10:c.1258+41_1258+42delinsTG MANE Select	ENSP00000265085.5:n.1258+41_1258+42delinsTG
ENST00000657000.1:c.-20-12426_-20-12425delinsTG	ENSP00000499433.1:n.-20-12426_-20-12425delinsTG
ENST00000659882.1:c.51+41_51+42delinsTG
ENST00000265085.9:c.1258+41_1258+42delinsTG	ENSP00000265085.5:n.1258+41_1258+42delinsTG
ENST00000334035.9:c.1208-10485_1208-10484delinsTG	ENSP00000334533.5:n.1208-10485_1208-10484delinsTG
ENST00000517880.1:c.62-12426_62-12425delinsTG	ENSP00000427990.1:n.62-12426_62-12425delinsTG
ENST00000519152.5:c.315+41_315+42delinsTG
ENST00000519467.1:n.40-10485_40-10484delinsTG
ENST00000519835.5:c.1208-12426_1208-12425delinsTG	ENSP00000429048.1:n.1208-12426_1208-12425delinsTG
ENST00000520867.5:c.1208-12426_1208-12425delinsTG	ENSP00000429092.1:n.1208-12426_1208-12425delinsTG
ENST00000522336.5:c.112+41_112+42delinsTG	ENSP00000430345.1:n.112+41_112+42delinsTG
NM_001308189.1:c.1208-10485_1208-10484delinsTG	NP_001295118.1:n.1208-10485_1208-10484delinsTG
NM_001308191.1:c.1208-12426_1208-12425delinsTG	NP_001295120.1:n.1208-12426_1208-12425delinsTG
NM_001308192.1:c.112+41_112+42delinsTG	NP_001295121.1:n.112+41_112+42delinsTG
NM_001308193.1:c.62-12426_62-12425delinsTG	NP_001295122.1:n.62-12426_62-12425delinsTG
NM_030627.2:c.1258+41_1258+42delinsTG	NP_085130.2:n.1258+41_1258+42delinsTG
NM_030627.3:c.1258+41_1258+42delinsTG	NP_085130.2:n.1258+41_1258+42delinsTG
XM_005265994.1:c.1258+41_1258+42delinsTG	XP_005266051.1:n.1258+41_1258+42delinsTG
XM_011534660.1:c.1258+41_1258+42delinsTG	XP_011532962.1:n.1258+41_1258+42delinsTG
XM_011534661.1:c.1208-10343_1208-10342delinsTG	XP_011532963.1:n.1208-10343_1208-10342delinsTG
XM_011534660.2:c.1258+41_1258+42delinsTG	XP_011532962.1:n.1258+41_1258+42delinsTG
XM_011534661.2:c.1208-10343_1208-10342delinsTG	XP_011532963.1:n.1208-10343_1208-10342delinsTG
NM_030627.4:c.1258+41_1258+42delinsTG MANE Select	NP_085130.2:n.1258+41_1258+42delinsTG
NM_001308189.2:c.1208-10485_1208-10484delinsTG	NP_001295118.1:n.1208-10485_1208-10484delinsTG
NM_001308191.2:c.1208-12426_1208-12425delinsTG	NP_001295120.1:n.1208-12426_1208-12425delinsTG
NM_001308192.2:c.112+41_112+42delinsTG	NP_001295121.1:n.112+41_112+42delinsTG
NM_001308193.2:c.62-12426_62-12425delinsTG	NP_001295122.1:n.62-12426_62-12425delinsTG