Canonical Allele Identifier: CA393148132

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710294A>G (hg19) ; chr15:g.74417953A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417953A>G , CM000677.2:g.74417953A>G	GRCh38
NC_000015.9:g.74710294A>G , CM000677.1:g.74710294A>G	GRCh37
NC_000015.8:g.72497347A>G	NCBI36
NG_011733.1:g.21006T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.389T>C MANE Select	ENSP00000261918.4:p.Ile130Thr
ENST00000542748.6:c.-107T>C	ENSP00000441493.1:n.-107T>C
ENST00000261918.8:c.389T>C	ENSP00000261918.4:p.Ile130Thr
ENST00000542748.5:c.-107T>C	ENSP00000441493.1:n.-107T>C
ENST00000543145.6:c.347T>C	ENSP00000438966.2:p.Ile116Thr
ENST00000567345.1:c.-107T>C	ENSP00000454365.1:n.-107T>C
NM_001146029.1:c.347T>C	NP_001139501.1:p.Ile116Thr
NM_001146030.1:c.-107T>C	NP_001139502.1:n.-107T>C
NM_003612.3:c.389T>C	NP_003603.1:p.Ile130Thr
NM_001146029.2:c.347T>C	NP_001139501.1:p.Ile116Thr
NM_001146030.2:c.-107T>C	NP_001139502.1:n.-107T>C
NM_003612.4:c.389T>C	NP_003603.1:p.Ile130Thr
NM_003612.5:c.389T>C MANE Select	NP_003603.1:p.Ile130Thr
NM_001146029.3:c.347T>C	NP_001139501.1:p.Ile116Thr
NM_001146030.3:c.-107T>C	NP_001139502.1:n.-107T>C