Canonical Allele Identifier: CA393148124

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710292T>C (hg19) ; chr15:g.74417951T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417951T>C , CM000677.2:g.74417951T>C	GRCh38
NC_000015.9:g.74710292T>C , CM000677.1:g.74710292T>C	GRCh37
NC_000015.8:g.72497345T>C	NCBI36
NG_011733.1:g.21008A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261918.9:c.391A>G MANE Select	ENSP00000261918.4:p.Thr131Ala
ENST00000542748.6:c.-105A>G	ENSP00000441493.1:n.-105A>G
ENST00000261918.8:c.391A>G	ENSP00000261918.4:p.Thr131Ala
ENST00000542748.5:c.-105A>G	ENSP00000441493.1:n.-105A>G
ENST00000543145.6:c.349A>G	ENSP00000438966.2:p.Thr117Ala
ENST00000567345.1:c.-105A>G	ENSP00000454365.1:n.-105A>G
NM_001146029.1:c.349A>G	NP_001139501.1:p.Thr117Ala
NM_001146030.1:c.-105A>G	NP_001139502.1:n.-105A>G
NM_003612.3:c.391A>G	NP_003603.1:p.Thr131Ala
NM_001146029.2:c.349A>G	NP_001139501.1:p.Thr117Ala
NM_001146030.2:c.-105A>G	NP_001139502.1:n.-105A>G
NM_003612.4:c.391A>G	NP_003603.1:p.Thr131Ala
NM_003612.5:c.391A>G MANE Select	NP_003603.1:p.Thr131Ala
NM_001146029.3:c.349A>G	NP_001139501.1:p.Thr117Ala
NM_001146030.3:c.-105A>G	NP_001139502.1:n.-105A>G