Canonical Allele Identifier: CA1721661766

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392482_83392484delinsTTA , CM000669.2:g.83392482_83392484delinsTTA	GRCh38
NC_000007.13:g.83021798_83021800delinsTTA , CM000669.1:g.83021798_83021800delinsTTA	GRCh37
NC_000007.12:g.82859734_82859736delinsTTA	NCBI36
NG_021242.1:g.261680_261682delinsTAA
NG_021242.2:g.261680_261682delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1487+71_1487+73delinsTAA	ENSP00000405052.1:n.1487+71_1487+73delinsTAA
ENST00000642232.1:c.1667+71_1667+73delinsTAA	ENSP00000494064.1:n.1667+71_1667+73delinsTAA
ENST00000643230.2:c.1667+71_1667+73delinsTAA MANE Select	ENSP00000496491.1:n.1667+71_1667+73delinsTAA
ENST00000643441.1:n.1652+71_1652+73delinsTAA
ENST00000307792.7:c.1667+71_1667+73delinsTAA	ENSP00000303212.3:n.1667+71_1667+73delinsTAA
ENST00000427262.5:c.1487+71_1487+73delinsTAA	ENSP00000405052.1:n.1487+71_1487+73delinsTAA
NM_001178129.1:c.1487+71_1487+73delinsTAA	NP_001171600.1:n.1487+71_1487+73delinsTAA
NM_012431.2:c.1667+71_1667+73delinsTAA	NP_036563.1:n.1667+71_1667+73delinsTAA
XM_011516715.1:c.1667+71_1667+73delinsTAA	XP_011515017.1:n.1667+71_1667+73delinsTAA
NM_012431.3:c.1667+71_1667+73delinsTAA MANE Select	NP_036563.1:n.1667+71_1667+73delinsTAA
NM_001178129.2:c.1487+71_1487+73delinsTAA	NP_001171600.1:n.1487+71_1487+73delinsTAA