Canonical Allele Identifier: CA491212793

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710233G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417892G>T , CM000677.2:g.74417892G>T	GRCh38
NC_000015.9:g.74710233G>T , CM000677.1:g.74710233G>T	GRCh37
NC_000015.8:g.72497286G>T	NCBI36
NG_011733.1:g.21067C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.450C>A MANE Select	ENSP00000261918.4:p.Pro150=
ENST00000542748.6:c.-46C>A	ENSP00000441493.1:n.-46C>A
ENST00000261918.8:c.450C>A	ENSP00000261918.4:p.Pro150=
ENST00000542748.5:c.-46C>A	ENSP00000441493.1:n.-46C>A
ENST00000543145.6:c.408C>A	ENSP00000438966.2:p.Pro136=
ENST00000567345.1:c.-46C>A	ENSP00000454365.1:n.-46C>A
NM_001146029.1:c.408C>A	NP_001139501.1:p.Pro136=
NM_001146030.1:c.-46C>A	NP_001139502.1:n.-46C>A
NM_003612.3:c.450C>A	NP_003603.1:p.Pro150=
NM_001146029.2:c.408C>A	NP_001139501.1:p.Pro136=
NM_001146030.2:c.-46C>A	NP_001139502.1:n.-46C>A
NM_003612.4:c.450C>A	NP_003603.1:p.Pro150=
NM_003612.5:c.450C>A MANE Select	NP_003603.1:p.Pro150=
NM_001146029.3:c.408C>A	NP_001139501.1:p.Pro136=
NM_001146030.3:c.-46C>A	NP_001139502.1:n.-46C>A