Canonical Allele Identifier: CA3564453

Gene: CPEB4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173890554T>G , CM000667.2:g.173890554T>G	GRCh38
NC_000005.9:g.173317557T>G , CM000667.1:g.173317557T>G	GRCh37
NC_000005.8:g.173250163T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265085.10:c.821T>G MANE Select	ENSP00000265085.5:p.Leu274Trp
ENST00000265085.9:c.821T>G	ENSP00000265085.5:p.Leu274Trp
ENST00000334035.9:c.821T>G	ENSP00000334533.5:p.Leu274Trp
ENST00000519835.5:c.821T>G	ENSP00000429048.1:p.Leu274Trp
ENST00000520867.5:c.821T>G	ENSP00000429092.1:p.Leu274Trp
NM_001308189.1:c.821T>G	NP_001295118.1:p.Leu274Trp
NM_001308191.1:c.821T>G	NP_001295120.1:p.Leu274Trp
NM_030627.2:c.821T>G	NP_085130.2:p.Leu274Trp
NM_030627.3:c.821T>G	NP_085130.2:p.Leu274Trp
XM_005265994.1:c.821T>G	XP_005266051.1:p.Leu274Trp
XM_011534660.1:c.821T>G	XP_011532962.1:p.Leu274Trp
XM_011534661.1:c.821T>G	XP_011532963.1:p.Leu274Trp
XM_011534660.2:c.821T>G	XP_011532962.1:p.Leu274Trp
XM_011534661.2:c.821T>G	XP_011532963.1:p.Leu274Trp
NM_030627.4:c.821T>G MANE Select	NP_085130.2:p.Leu274Trp
NM_001308189.2:c.821T>G	NP_001295118.1:p.Leu274Trp
NM_001308191.2:c.821T>G	NP_001295120.1:p.Leu274Trp