Canonical Allele Identifier: CA7657268
Gene: SEMA7A HGNC NCBI

Linked Data

dbSNP Id: rs750229375

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74417959T>C , CM000677.2:g.74417959T>C GRCh38
NC_000015.9:g.74710300T>C , CM000677.1:g.74710300T>C GRCh37
NC_000015.8:g.72497353T>C NCBI36
NG_011733.1:g.21000A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261918.9:c.383A>G MANE Select ENSP00000261918.4:p.Asn128Ser
ENST00000542748.6:c.-113A>G ENSP00000441493.1:n.-113A>G
ENST00000261918.8:c.383A>G ENSP00000261918.4:p.Asn128Ser
ENST00000542748.5:c.-113A>G ENSP00000441493.1:n.-113A>G
ENST00000543145.6:c.341A>G ENSP00000438966.2:p.Asn114Ser
ENST00000567345.1:c.-113A>G ENSP00000454365.1:n.-113A>G
NM_001146029.1:c.341A>G NP_001139501.1:p.Asn114Ser
NM_001146030.1:c.-113A>G NP_001139502.1:n.-113A>G
NM_003612.3:c.383A>G NP_003603.1:p.Asn128Ser
NM_001146029.2:c.341A>G NP_001139501.1:p.Asn114Ser
NM_001146030.2:c.-113A>G NP_001139502.1:n.-113A>G
NM_003612.4:c.383A>G NP_003603.1:p.Asn128Ser
NM_003612.5:c.383A>G MANE Select NP_003603.1:p.Asn128Ser
NM_001146029.3:c.341A>G NP_001139501.1:p.Asn114Ser
NM_001146030.3:c.-113A>G NP_001139502.1:n.-113A>G