Canonical Allele Identifier: CA2187679205

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417936_74417937delinsGC , CM000677.2:g.74417936_74417937delinsGC	GRCh38
NC_000015.9:g.74710277_74710278delinsGC , CM000677.1:g.74710277_74710278delinsGC	GRCh37
NC_000015.8:g.72497330_72497331delinsGC	NCBI36
NG_011733.1:g.21022_21023delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.405_406delinsGC MANE Select	ENSP00000261918.4:p.Arg135=
ENST00000542748.6:c.-91_-90delinsGC	ENSP00000441493.1:n.-91_-90delinsGC
ENST00000261918.8:c.405_406delinsGC	ENSP00000261918.4:p.Arg135=
ENST00000542748.5:c.-91_-90delinsGC	ENSP00000441493.1:n.-91_-90delinsGC
ENST00000543145.6:c.363_364delinsGC	ENSP00000438966.2:p.Arg121=
ENST00000567345.1:c.-91_-90delinsGC	ENSP00000454365.1:n.-91_-90delinsGC
NM_001146029.1:c.363_364delinsGC	NP_001139501.1:p.Arg121=
NM_001146030.1:c.-91_-90delinsGC	NP_001139502.1:n.-91_-90delinsGC
NM_003612.3:c.405_406delinsGC	NP_003603.1:p.Arg135=
NM_001146029.2:c.363_364delinsGC	NP_001139501.1:p.Arg121=
NM_001146030.2:c.-91_-90delinsGC	NP_001139502.1:n.-91_-90delinsGC
NM_003612.4:c.405_406delinsGC	NP_003603.1:p.Arg135=
NM_003612.5:c.405_406delinsGC MANE Select	NP_003603.1:p.Arg135=
NM_001146029.3:c.363_364delinsGC	NP_001139501.1:p.Arg121=
NM_001146030.3:c.-91_-90delinsGC	NP_001139502.1:n.-91_-90delinsGC