Canonical Allele Identifier: CA2839445581

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417908del , CM000677.2:g.74417908del	GRCh38
NC_000015.9:g.74710249del , CM000677.1:g.74710249del	GRCh37
NC_000015.8:g.72497302del	NCBI36
NG_011733.1:g.21052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.435del MANE Select	ENSP00000261918.4:p.Asn146ThrfsTer11
ENST00000542748.6:c.-61del	ENSP00000441493.1:n.-61del
ENST00000261918.8:c.435del	ENSP00000261918.4:p.Asn146ThrfsTer11
ENST00000542748.5:c.-61del	ENSP00000441493.1:n.-61del
ENST00000543145.6:c.393del	ENSP00000438966.2:p.Asn132ThrfsTer11
ENST00000567345.1:c.-61del	ENSP00000454365.1:n.-61del
NM_001146029.1:c.393del	NP_001139501.1:p.Asn132ThrfsTer11
NM_001146030.1:c.-61del	NP_001139502.1:n.-61del
NM_003612.3:c.435del	NP_003603.1:p.Asn146ThrfsTer11
NM_001146029.2:c.393del	NP_001139501.1:p.Asn132ThrfsTer11
NM_001146030.2:c.-61del	NP_001139502.1:n.-61del
NM_003612.4:c.435del	NP_003603.1:p.Asn146ThrfsTer11
NM_003612.5:c.435del MANE Select	NP_003603.1:p.Asn146ThrfsTer11
NM_001146029.3:c.393del	NP_001139501.1:p.Asn132ThrfsTer11
NM_001146030.3:c.-61del	NP_001139502.1:n.-61del