Canonical Allele Identifier: CA2187679221

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417944A= , CM000677.2:g.74417944A=	GRCh38
NC_000015.9:g.74710285A= , CM000677.1:g.74710285A=	GRCh37
NC_000015.8:g.72497338A=	NCBI36
NG_011733.1:g.21015T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.398T= MANE Select	ENSP00000261918.4:p.Leu133=
ENST00000542748.6:c.-98T=	ENSP00000441493.1:n.-98T=
ENST00000261918.8:c.398T=	ENSP00000261918.4:p.Leu133=
ENST00000542748.5:c.-98T=	ENSP00000441493.1:n.-98T=
ENST00000543145.6:c.356T=	ENSP00000438966.2:p.Leu119=
ENST00000567345.1:c.-98T=	ENSP00000454365.1:n.-98T=
NM_001146029.1:c.356T=	NP_001139501.1:p.Leu119=
NM_001146030.1:c.-98T=	NP_001139502.1:n.-98T=
NM_003612.3:c.398T=	NP_003603.1:p.Leu133=
NM_001146029.2:c.356T=	NP_001139501.1:p.Leu119=
NM_001146030.2:c.-98T=	NP_001139502.1:n.-98T=
NM_003612.4:c.398T=	NP_003603.1:p.Leu133=
NM_003612.5:c.398T= MANE Select	NP_003603.1:p.Leu133=
NM_001146029.3:c.356T=	NP_001139501.1:p.Leu119=
NM_001146030.3:c.-98T=	NP_001139502.1:n.-98T=