Canonical Allele Identifier: CA1601985803
Gene: CPEB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173932720_173932721delinsCA , CM000667.2:g.173932720_173932721delinsCA GRCh38
NC_000005.9:g.173359723_173359724delinsCA , CM000667.1:g.173359723_173359724delinsCA GRCh37
NC_000005.8:g.173292329_173292330delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265085.10:c.1258+220_1258+221delinsCA MANE Select ENSP00000265085.5:n.1258+220_1258+221delinsCA
ENST00000657000.1:c.-20-12247_-20-12246delinsCA ENSP00000499433.1:n.-20-12247_-20-12246delinsCA
ENST00000659882.1:c.51+220_51+221delinsCA
ENST00000265085.9:c.1258+220_1258+221delinsCA ENSP00000265085.5:n.1258+220_1258+221delinsCA
ENST00000334035.9:c.1208-10306_1208-10305delinsCA ENSP00000334533.5:n.1208-10306_1208-10305delinsCA
ENST00000517880.1:c.62-12247_62-12246delinsCA ENSP00000427990.1:n.62-12247_62-12246delinsCA
ENST00000519152.5:c.315+220_315+221delinsCA
ENST00000519467.1:n.40-10306_40-10305delinsCA
ENST00000519835.5:c.1208-12247_1208-12246delinsCA ENSP00000429048.1:n.1208-12247_1208-12246delinsCA
ENST00000520867.5:c.1208-12247_1208-12246delinsCA ENSP00000429092.1:n.1208-12247_1208-12246delinsCA
ENST00000522336.5:c.112+220_112+221delinsCA ENSP00000430345.1:n.112+220_112+221delinsCA
NM_001308189.1:c.1208-10306_1208-10305delinsCA NP_001295118.1:n.1208-10306_1208-10305delinsCA
NM_001308191.1:c.1208-12247_1208-12246delinsCA NP_001295120.1:n.1208-12247_1208-12246delinsCA
NM_001308192.1:c.112+220_112+221delinsCA NP_001295121.1:n.112+220_112+221delinsCA
NM_001308193.1:c.62-12247_62-12246delinsCA NP_001295122.1:n.62-12247_62-12246delinsCA
NM_030627.2:c.1258+220_1258+221delinsCA NP_085130.2:n.1258+220_1258+221delinsCA
NM_030627.3:c.1258+220_1258+221delinsCA NP_085130.2:n.1258+220_1258+221delinsCA
XM_005265994.1:c.1258+220_1258+221delinsCA XP_005266051.1:n.1258+220_1258+221delinsCA
XM_011534660.1:c.1258+220_1258+221delinsCA XP_011532962.1:n.1258+220_1258+221delinsCA
XM_011534661.1:c.1208-10164_1208-10163delinsCA XP_011532963.1:n.1208-10164_1208-10163delinsCA
XM_011534660.2:c.1258+220_1258+221delinsCA XP_011532962.1:n.1258+220_1258+221delinsCA
XM_011534661.2:c.1208-10164_1208-10163delinsCA XP_011532963.1:n.1208-10164_1208-10163delinsCA
NM_030627.4:c.1258+220_1258+221delinsCA MANE Select NP_085130.2:n.1258+220_1258+221delinsCA
NM_001308189.2:c.1208-10306_1208-10305delinsCA NP_001295118.1:n.1208-10306_1208-10305delinsCA
NM_001308191.2:c.1208-12247_1208-12246delinsCA NP_001295120.1:n.1208-12247_1208-12246delinsCA
NM_001308192.2:c.112+220_112+221delinsCA NP_001295121.1:n.112+220_112+221delinsCA
NM_001308193.2:c.62-12247_62-12246delinsCA NP_001295122.1:n.62-12247_62-12246delinsCA