Canonical Allele Identifier: CA491212848

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710290A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417949A>C , CM000677.2:g.74417949A>C	GRCh38
NC_000015.9:g.74710290A>C , CM000677.1:g.74710290A>C	GRCh37
NC_000015.8:g.72497343A>C	NCBI36
NG_011733.1:g.21010T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261918.9:c.393T>G MANE Select	ENSP00000261918.4:p.Thr131=
ENST00000542748.6:c.-103T>G	ENSP00000441493.1:n.-103T>G
ENST00000261918.8:c.393T>G	ENSP00000261918.4:p.Thr131=
ENST00000542748.5:c.-103T>G	ENSP00000441493.1:n.-103T>G
ENST00000543145.6:c.351T>G	ENSP00000438966.2:p.Thr117=
ENST00000567345.1:c.-103T>G	ENSP00000454365.1:n.-103T>G
NM_001146029.1:c.351T>G	NP_001139501.1:p.Thr117=
NM_001146030.1:c.-103T>G	NP_001139502.1:n.-103T>G
NM_003612.3:c.393T>G	NP_003603.1:p.Thr131=
NM_001146029.2:c.351T>G	NP_001139501.1:p.Thr117=
NM_001146030.2:c.-103T>G	NP_001139502.1:n.-103T>G
NM_003612.4:c.393T>G	NP_003603.1:p.Thr131=
NM_003612.5:c.393T>G MANE Select	NP_003603.1:p.Thr131=
NM_001146029.3:c.351T>G	NP_001139501.1:p.Thr117=
NM_001146030.3:c.-103T>G	NP_001139502.1:n.-103T>G