Canonical Allele Identifier: CA272789800

Gene: SEMA7A

Linked Data

• dbSNP Id: rs1003304924
• gnomAD v2: 15-74710244-C-T
• gnomAD v4: 15-74417903-C-T
• MyVariant Identifiers: chr15:g.74710244C>T (hg19) ; chr15:g.74417903C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417903C>T , CM000677.2:g.74417903C>T	GRCh38
NC_000015.9:g.74710244C>T , CM000677.1:g.74710244C>T	GRCh37
NC_000015.8:g.72497297C>T	NCBI36
NG_011733.1:g.21056G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.439G>A MANE Select	ENSP00000261918.4:p.Ala147Thr
ENST00000542748.6:c.-57G>A	ENSP00000441493.1:n.-57G>A
ENST00000261918.8:c.439G>A	ENSP00000261918.4:p.Ala147Thr
ENST00000542748.5:c.-57G>A	ENSP00000441493.1:n.-57G>A
ENST00000543145.6:c.397G>A	ENSP00000438966.2:p.Ala133Thr
ENST00000567345.1:c.-57G>A	ENSP00000454365.1:n.-57G>A
NM_001146029.1:c.397G>A	NP_001139501.1:p.Ala133Thr
NM_001146030.1:c.-57G>A	NP_001139502.1:n.-57G>A
NM_003612.3:c.439G>A	NP_003603.1:p.Ala147Thr
NM_001146029.2:c.397G>A	NP_001139501.1:p.Ala133Thr
NM_001146030.2:c.-57G>A	NP_001139502.1:n.-57G>A
NM_003612.4:c.439G>A	NP_003603.1:p.Ala147Thr
NM_003612.5:c.439G>A MANE Select	NP_003603.1:p.Ala147Thr
NM_001146029.3:c.397G>A	NP_001139501.1:p.Ala133Thr
NM_001146030.3:c.-57G>A	NP_001139502.1:n.-57G>A