Canonical Allele Identifier: CA2841542032

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417941del , CM000677.2:g.74417941del	GRCh38
NC_000015.9:g.74710282del , CM000677.1:g.74710282del	GRCh37
NC_000015.8:g.72497335del	NCBI36
NG_011733.1:g.21018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.401del MANE Select	ENSP00000261918.4:p.Glu134GlyfsTer23
ENST00000542748.6:c.-95del	ENSP00000441493.1:n.-95del
ENST00000261918.8:c.401del	ENSP00000261918.4:p.Glu134GlyfsTer23
ENST00000542748.5:c.-95del	ENSP00000441493.1:n.-95del
ENST00000543145.6:c.359del	ENSP00000438966.2:p.Glu120GlyfsTer23
ENST00000567345.1:c.-95del	ENSP00000454365.1:n.-95del
NM_001146029.1:c.359del	NP_001139501.1:p.Glu120GlyfsTer23
NM_001146030.1:c.-95del	NP_001139502.1:n.-95del
NM_003612.3:c.401del	NP_003603.1:p.Glu134GlyfsTer23
NM_001146029.2:c.359del	NP_001139501.1:p.Glu120GlyfsTer23
NM_001146030.2:c.-95del	NP_001139502.1:n.-95del
NM_003612.4:c.401del	NP_003603.1:p.Glu134GlyfsTer23
NM_003612.5:c.401del MANE Select	NP_003603.1:p.Glu134GlyfsTer23
NM_001146029.3:c.359del	NP_001139501.1:p.Glu120GlyfsTer23
NM_001146030.3:c.-95del	NP_001139502.1:n.-95del