Canonical Allele Identifier: CA2187679228

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417952G= , CM000677.2:g.74417952G=	GRCh38
NC_000015.9:g.74710293G= , CM000677.1:g.74710293G=	GRCh37
NC_000015.8:g.72497346G=	NCBI36
NG_011733.1:g.21007C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.390C= MANE Select	ENSP00000261918.4:p.Ile130=
ENST00000542748.6:c.-106C=	ENSP00000441493.1:n.-106C=
ENST00000261918.8:c.390C=	ENSP00000261918.4:p.Ile130=
ENST00000542748.5:c.-106C=	ENSP00000441493.1:n.-106C=
ENST00000543145.6:c.348C=	ENSP00000438966.2:p.Ile116=
ENST00000567345.1:c.-106C=	ENSP00000454365.1:n.-106C=
NM_001146029.1:c.348C=	NP_001139501.1:p.Ile116=
NM_001146030.1:c.-106C=	NP_001139502.1:n.-106C=
NM_003612.3:c.390C=	NP_003603.1:p.Ile130=
NM_001146029.2:c.348C=	NP_001139501.1:p.Ile116=
NM_001146030.2:c.-106C=	NP_001139502.1:n.-106C=
NM_003612.4:c.390C=	NP_003603.1:p.Ile130=
NM_003612.5:c.390C= MANE Select	NP_003603.1:p.Ile130=
NM_001146029.3:c.348C=	NP_001139501.1:p.Ile116=
NM_001146030.3:c.-106C=	NP_001139502.1:n.-106C=