Canonical Allele Identifier: CA393147902

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710236G>T (hg19) ; chr15:g.74417895G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417895G>T , CM000677.2:g.74417895G>T	GRCh38
NC_000015.9:g.74710236G>T , CM000677.1:g.74710236G>T	GRCh37
NC_000015.8:g.72497289G>T	NCBI36
NG_011733.1:g.21064C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.447C>A MANE Select	ENSP00000261918.4:p.His149Gln
ENST00000542748.6:c.-49C>A	ENSP00000441493.1:n.-49C>A
ENST00000261918.8:c.447C>A	ENSP00000261918.4:p.His149Gln
ENST00000542748.5:c.-49C>A	ENSP00000441493.1:n.-49C>A
ENST00000543145.6:c.405C>A	ENSP00000438966.2:p.His135Gln
ENST00000567345.1:c.-49C>A	ENSP00000454365.1:n.-49C>A
NM_001146029.1:c.405C>A	NP_001139501.1:p.His135Gln
NM_001146030.1:c.-49C>A	NP_001139502.1:n.-49C>A
NM_003612.3:c.447C>A	NP_003603.1:p.His149Gln
NM_001146029.2:c.405C>A	NP_001139501.1:p.His135Gln
NM_001146030.2:c.-49C>A	NP_001139502.1:n.-49C>A
NM_003612.4:c.447C>A	NP_003603.1:p.His149Gln
NM_003612.5:c.447C>A MANE Select	NP_003603.1:p.His149Gln
NM_001146029.3:c.405C>A	NP_001139501.1:p.His135Gln
NM_001146030.3:c.-49C>A	NP_001139502.1:n.-49C>A