Canonical Allele Identifier: CA2187679192

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417933T= , CM000677.2:g.74417933T=	GRCh38
NC_000015.9:g.74710274T= , CM000677.1:g.74710274T=	GRCh37
NC_000015.8:g.72497327T=	NCBI36
NG_011733.1:g.21026A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.409A= MANE Select	ENSP00000261918.4:p.Ser137=
ENST00000542748.6:c.-87A=	ENSP00000441493.1:n.-87A=
ENST00000261918.8:c.409A=	ENSP00000261918.4:p.Ser137=
ENST00000542748.5:c.-87A=	ENSP00000441493.1:n.-87A=
ENST00000543145.6:c.367A=	ENSP00000438966.2:p.Ser123=
ENST00000567345.1:c.-87A=	ENSP00000454365.1:n.-87A=
NM_001146029.1:c.367A=	NP_001139501.1:p.Ser123=
NM_001146030.1:c.-87A=	NP_001139502.1:n.-87A=
NM_003612.3:c.409A=	NP_003603.1:p.Ser137=
NM_001146029.2:c.367A=	NP_001139501.1:p.Ser123=
NM_001146030.2:c.-87A=	NP_001139502.1:n.-87A=
NM_003612.4:c.409A=	NP_003603.1:p.Ser137=
NM_003612.5:c.409A= MANE Select	NP_003603.1:p.Ser137=
NM_001146029.3:c.367A=	NP_001139501.1:p.Ser123=
NM_001146030.3:c.-87A=	NP_001139502.1:n.-87A=