Canonical Allele Identifier: CA2187679196

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417935C= , CM000677.2:g.74417935C=	GRCh38
NC_000015.9:g.74710276C= , CM000677.1:g.74710276C=	GRCh37
NC_000015.8:g.72497329C=	NCBI36
NG_011733.1:g.21024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.407G= MANE Select	ENSP00000261918.4:p.Arg136=
ENST00000542748.6:c.-89G=	ENSP00000441493.1:n.-89G=
ENST00000261918.8:c.407G=	ENSP00000261918.4:p.Arg136=
ENST00000542748.5:c.-89G=	ENSP00000441493.1:n.-89G=
ENST00000543145.6:c.365G=	ENSP00000438966.2:p.Arg122=
ENST00000567345.1:c.-89G=	ENSP00000454365.1:n.-89G=
NM_001146029.1:c.365G=	NP_001139501.1:p.Arg122=
NM_001146030.1:c.-89G=	NP_001139502.1:n.-89G=
NM_003612.3:c.407G=	NP_003603.1:p.Arg136=
NM_001146029.2:c.365G=	NP_001139501.1:p.Arg122=
NM_001146030.2:c.-89G=	NP_001139502.1:n.-89G=
NM_003612.4:c.407G=	NP_003603.1:p.Arg136=
NM_003612.5:c.407G= MANE Select	NP_003603.1:p.Arg136=
NM_001146029.3:c.365G=	NP_001139501.1:p.Arg122=
NM_001146030.3:c.-89G=	NP_001139502.1:n.-89G=