Canonical Allele Identifier: CA1103848113
Gene: SEMA3E HGNC NCBI

Linked Data

dbSNP Id: rs1788037485

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392481_83392484del , CM000669.2:g.83392481_83392484del GRCh38
NC_000007.13:g.83021797_83021800del , CM000669.1:g.83021797_83021800del GRCh37
NC_000007.12:g.82859733_82859736del NCBI36
NG_021242.1:g.261681_261684del
NG_021242.2:g.261681_261684del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1487+72_1487+75del ENSP00000405052.1:n.1487+72_1487+75del
ENST00000642232.1:c.1667+72_1667+75del ENSP00000494064.1:n.1667+72_1667+75del
ENST00000643230.2:c.1667+72_1667+75del MANE Select ENSP00000496491.1:n.1667+72_1667+75del
ENST00000643441.1:n.1652+72_1652+75del
ENST00000307792.7:c.1667+72_1667+75del ENSP00000303212.3:n.1667+72_1667+75del
ENST00000427262.5:c.1487+72_1487+75del ENSP00000405052.1:n.1487+72_1487+75del
NM_001178129.1:c.1487+72_1487+75del NP_001171600.1:n.1487+72_1487+75del
NM_012431.2:c.1667+72_1667+75del NP_036563.1:n.1667+72_1667+75del
XM_011516715.1:c.1667+72_1667+75del XP_011515017.1:n.1667+72_1667+75del
NM_012431.3:c.1667+72_1667+75del MANE Select NP_036563.1:n.1667+72_1667+75del
NM_001178129.2:c.1487+72_1487+75del NP_001171600.1:n.1487+72_1487+75del