Canonical Allele Identifier: CA393148151

Gene: SEMA7A

Linked Data

• dbSNP Id: rs2060966548
• gnomAD v4: 15-74417957-A-C
• MyVariant Identifiers: chr15:g.74710298A>C (hg19) ; chr15:g.74417957A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417957A>C , CM000677.2:g.74417957A>C	GRCh38
NC_000015.9:g.74710298A>C , CM000677.1:g.74710298A>C	GRCh37
NC_000015.8:g.72497351A>C	NCBI36
NG_011733.1:g.21002T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.385T>G MANE Select	ENSP00000261918.4:p.Tyr129Asp
ENST00000542748.6:c.-111T>G	ENSP00000441493.1:n.-111T>G
ENST00000261918.8:c.385T>G	ENSP00000261918.4:p.Tyr129Asp
ENST00000542748.5:c.-111T>G	ENSP00000441493.1:n.-111T>G
ENST00000543145.6:c.343T>G	ENSP00000438966.2:p.Tyr115Asp
ENST00000567345.1:c.-111T>G	ENSP00000454365.1:n.-111T>G
NM_001146029.1:c.343T>G	NP_001139501.1:p.Tyr115Asp
NM_001146030.1:c.-111T>G	NP_001139502.1:n.-111T>G
NM_003612.3:c.385T>G	NP_003603.1:p.Tyr129Asp
NM_001146029.2:c.343T>G	NP_001139501.1:p.Tyr115Asp
NM_001146030.2:c.-111T>G	NP_001139502.1:n.-111T>G
NM_003612.4:c.385T>G	NP_003603.1:p.Tyr129Asp
NM_003612.5:c.385T>G MANE Select	NP_003603.1:p.Tyr129Asp
NM_001146029.3:c.343T>G	NP_001139501.1:p.Tyr115Asp
NM_001146030.3:c.-111T>G	NP_001139502.1:n.-111T>G