Canonical Allele Identifier: CA1601985441
Gene: CPEB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173932418T= , CM000667.2:g.173932418T= GRCh38
NC_000005.9:g.173359421T= , CM000667.1:g.173359421T= GRCh37
NC_000005.8:g.173292027T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265085.10:c.1208-32T= MANE Select ENSP00000265085.5:n.1208-32T=
ENST00000657000.1:c.-20-12549T= ENSP00000499433.1:n.-20-12549T=
ENST00000265085.9:c.1208-32T= ENSP00000265085.5:n.1208-32T=
ENST00000334035.9:c.1208-10608T= ENSP00000334533.5:n.1208-10608T=
ENST00000517880.1:c.62-12549T= ENSP00000427990.1:n.62-12549T=
ENST00000519152.5:c.265-32T=
ENST00000519467.1:n.40-10608T=
ENST00000519835.5:c.1208-12549T= ENSP00000429048.1:n.1208-12549T=
ENST00000520867.5:c.1208-12549T= ENSP00000429092.1:n.1208-12549T=
ENST00000522336.5:c.62-32T= ENSP00000430345.1:n.62-32T=
NM_001308189.1:c.1208-10608T= NP_001295118.1:n.1208-10608T=
NM_001308191.1:c.1208-12549T= NP_001295120.1:n.1208-12549T=
NM_001308192.1:c.62-32T= NP_001295121.1:n.62-32T=
NM_001308193.1:c.62-12549T= NP_001295122.1:n.62-12549T=
NM_030627.2:c.1208-32T= NP_085130.2:n.1208-32T=
NM_030627.3:c.1208-32T= NP_085130.2:n.1208-32T=
XM_005265994.1:c.1208-32T= XP_005266051.1:n.1208-32T=
XM_011534660.1:c.1208-32T= XP_011532962.1:n.1208-32T=
XM_011534661.1:c.1208-10466T= XP_011532963.1:n.1208-10466T=
XM_011534660.2:c.1208-32T= XP_011532962.1:n.1208-32T=
XM_011534661.2:c.1208-10466T= XP_011532963.1:n.1208-10466T=
NM_030627.4:c.1208-32T= MANE Select NP_085130.2:n.1208-32T=
NM_001308189.2:c.1208-10608T= NP_001295118.1:n.1208-10608T=
NM_001308191.2:c.1208-12549T= NP_001295120.1:n.1208-12549T=
NM_001308192.2:c.62-32T= NP_001295121.1:n.62-32T=
NM_001308193.2:c.62-12549T= NP_001295122.1:n.62-12549T=