Canonical Allele Identifier: CA1721679672

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407489_83407492delinsGAGA , CM000669.2:g.83407489_83407492delinsGAGA	GRCh38
NC_000007.13:g.83036805_83036808delinsGAGA , CM000669.1:g.83036805_83036808delinsGAGA	GRCh37
NC_000007.12:g.82874741_82874744delinsGAGA	NCBI36
NG_021242.1:g.246672_246675delinsTCTC
NG_021242.2:g.246672_246675delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.491-253_491-250delinsTCTC	ENSP00000405052.1:n.491-253_491-250delinsTCTC
ENST00000642232.1:c.671-253_671-250delinsTCTC	ENSP00000494064.1:n.671-253_671-250delinsTCTC
ENST00000643230.2:c.671-253_671-250delinsTCTC MANE Select	ENSP00000496491.1:n.671-253_671-250delinsTCTC
ENST00000643441.1:n.656-253_656-250delinsTCTC
ENST00000644381.1:n.234-253_234-250delinsTCTC
ENST00000307792.7:c.671-253_671-250delinsTCTC	ENSP00000303212.3:n.671-253_671-250delinsTCTC
ENST00000427262.5:c.491-253_491-250delinsTCTC	ENSP00000405052.1:n.491-253_491-250delinsTCTC
NM_001178129.1:c.491-253_491-250delinsTCTC	NP_001171600.1:n.491-253_491-250delinsTCTC
NM_012431.2:c.671-253_671-250delinsTCTC	NP_036563.1:n.671-253_671-250delinsTCTC
XM_011516715.1:c.671-253_671-250delinsTCTC	XP_011515017.1:n.671-253_671-250delinsTCTC
NM_012431.3:c.671-253_671-250delinsTCTC MANE Select	NP_036563.1:n.671-253_671-250delinsTCTC
NM_001178129.2:c.491-253_491-250delinsTCTC	NP_001171600.1:n.491-253_491-250delinsTCTC