Canonical Allele Identifier: CA491212790

Gene: SEMA7A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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