Canonical Allele Identifier: CA2187679165

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417909T= , CM000677.2:g.74417909T=	GRCh38
NC_000015.9:g.74710250T= , CM000677.1:g.74710250T=	GRCh37
NC_000015.8:g.72497303T=	NCBI36
NG_011733.1:g.21050A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.433A= MANE Select	ENSP00000261918.4:p.Thr145=
ENST00000542748.6:c.-63A=	ENSP00000441493.1:n.-63A=
ENST00000261918.8:c.433A=	ENSP00000261918.4:p.Thr145=
ENST00000542748.5:c.-63A=	ENSP00000441493.1:n.-63A=
ENST00000543145.6:c.391A=	ENSP00000438966.2:p.Thr131=
ENST00000567345.1:c.-63A=	ENSP00000454365.1:n.-63A=
NM_001146029.1:c.391A=	NP_001139501.1:p.Thr131=
NM_001146030.1:c.-63A=	NP_001139502.1:n.-63A=
NM_003612.3:c.433A=	NP_003603.1:p.Thr145=
NM_001146029.2:c.391A=	NP_001139501.1:p.Thr131=
NM_001146030.2:c.-63A=	NP_001139502.1:n.-63A=
NM_003612.4:c.433A=	NP_003603.1:p.Thr145=
NM_003612.5:c.433A= MANE Select	NP_003603.1:p.Thr145=
NM_001146029.3:c.391A=	NP_001139501.1:p.Thr131=
NM_001146030.3:c.-63A=	NP_001139502.1:n.-63A=