Canonical Allele Identifier: CA2187679433

Gene: SEMA7A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74418149C= , CM000677.2:g.74418149C=	GRCh38
NC_000015.9:g.74710490C= , CM000677.1:g.74710490C=	GRCh37
NC_000015.8:g.72497543C=	NCBI36
NG_011733.1:g.20810G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261918.9:c.372+119G= MANE Select	ENSP00000261918.4:n.372+119G=
ENST00000542748.6:c.-124+119G=	ENSP00000441493.1:n.-124+119G=
ENST00000261918.8:c.372+119G=	ENSP00000261918.4:n.372+119G=
ENST00000542748.5:c.-124+119G=	ENSP00000441493.1:n.-124+119G=
ENST00000543145.6:c.331-180G=	ENSP00000438966.2:n.331-180G=
ENST00000567345.1:c.-124+119G=	ENSP00000454365.1:n.-124+119G=
NM_001146029.1:c.331-180G=	NP_001139501.1:n.331-180G=
NM_001146030.1:c.-124+119G=	NP_001139502.1:n.-124+119G=
NM_003612.3:c.372+119G=	NP_003603.1:n.372+119G=
NM_001146029.2:c.331-180G=	NP_001139501.1:n.331-180G=
NM_001146030.2:c.-124+119G=	NP_001139502.1:n.-124+119G=
NM_003612.4:c.372+119G=	NP_003603.1:n.372+119G=
NM_003612.5:c.372+119G= MANE Select	NP_003603.1:n.372+119G=
NM_001146029.3:c.331-180G=	NP_001139501.1:n.331-180G=
NM_001146030.3:c.-124+119G=	NP_001139502.1:n.-124+119G=