Canonical Allele Identifier: CA491212810

Gene: SEMA7A

Linked Data

• gnomAD v4: 15-74417916-G-C
• MyVariant Identifiers: chr15:g.74710257G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417916G>C , CM000677.2:g.74417916G>C	GRCh38
NC_000015.9:g.74710257G>C , CM000677.1:g.74710257G>C	GRCh37
NC_000015.8:g.72497310G>C	NCBI36
NG_011733.1:g.21043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.426C>G MANE Select	ENSP00000261918.4:p.Ala142=
ENST00000542748.6:c.-70C>G	ENSP00000441493.1:n.-70C>G
ENST00000261918.8:c.426C>G	ENSP00000261918.4:p.Ala142=
ENST00000542748.5:c.-70C>G	ENSP00000441493.1:n.-70C>G
ENST00000543145.6:c.384C>G	ENSP00000438966.2:p.Ala128=
ENST00000567345.1:c.-70C>G	ENSP00000454365.1:n.-70C>G
NM_001146029.1:c.384C>G	NP_001139501.1:p.Ala128=
NM_001146030.1:c.-70C>G	NP_001139502.1:n.-70C>G
NM_003612.3:c.426C>G	NP_003603.1:p.Ala142=
NM_001146029.2:c.384C>G	NP_001139501.1:p.Ala128=
NM_001146030.2:c.-70C>G	NP_001139502.1:n.-70C>G
NM_003612.4:c.426C>G	NP_003603.1:p.Ala142=
NM_003612.5:c.426C>G MANE Select	NP_003603.1:p.Ala142=
NM_001146029.3:c.384C>G	NP_001139501.1:p.Ala128=
NM_001146030.3:c.-70C>G	NP_001139502.1:n.-70C>G