Canonical Allele Identifier: CA1721679582
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407285C= , CM000669.2:g.83407285C= GRCh38
NC_000007.13:g.83036601C= , CM000669.1:g.83036601C= GRCh37
NC_000007.12:g.82874537C= NCBI36
NG_021242.1:g.246879G=
NG_021242.2:g.246879G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.491-46G= ENSP00000405052.1:n.491-46G=
ENST00000642232.1:c.671-46G= ENSP00000494064.1:n.671-46G=
ENST00000643230.2:c.671-46G= MANE Select ENSP00000496491.1:n.671-46G=
ENST00000643441.1:n.656-46G=
ENST00000644381.1:n.234-46G=
ENST00000307792.7:c.671-46G= ENSP00000303212.3:n.671-46G=
ENST00000427262.5:c.491-46G= ENSP00000405052.1:n.491-46G=
NM_001178129.1:c.491-46G= NP_001171600.1:n.491-46G=
NM_012431.2:c.671-46G= NP_036563.1:n.671-46G=
XM_011516715.1:c.671-46G= XP_011515017.1:n.671-46G=
NM_012431.3:c.671-46G= MANE Select NP_036563.1:n.671-46G=
NM_001178129.2:c.491-46G= NP_001171600.1:n.491-46G=