Canonical Allele Identifier: CA1721679492

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407101_83407103delinsCAG , CM000669.2:g.83407101_83407103delinsCAG	GRCh38
NC_000007.13:g.83036417_83036419delinsCAG , CM000669.1:g.83036417_83036419delinsCAG	GRCh37
NC_000007.12:g.82874353_82874355delinsCAG	NCBI36
NG_021242.1:g.247061_247063delinsCTG
NG_021242.2:g.247061_247063delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000427262.6:c.627_629delinsCTG	ENSP00000405052.1:p.Leu209=
ENST00000642232.1:c.807_809delinsCTG	ENSP00000494064.1:p.Leu269=
ENST00000643230.2:c.807_809delinsCTG MANE Select	ENSP00000496491.1:p.Leu269=
ENST00000643441.1:n.792_794delinsCTG
ENST00000307792.7:c.807_809delinsCTG	ENSP00000303212.3:p.Leu269=
ENST00000427262.5:c.627_629delinsCTG	ENSP00000405052.1:p.Leu209=
NM_001178129.1:c.627_629delinsCTG	NP_001171600.1:p.Leu209=
NM_012431.2:c.807_809delinsCTG	NP_036563.1:p.Leu269=
XM_011516715.1:c.807_809delinsCTG	XP_011515017.1:p.Leu269=
NM_012431.3:c.807_809delinsCTG MANE Select	NP_036563.1:p.Leu269=
NM_001178129.2:c.627_629delinsCTG	NP_001171600.1:p.Leu209=