Canonical Allele Identifier: CA393147943

Gene: SEMA7A

Linked Data

• MyVariant Identifiers: chr15:g.74710246T>G (hg19) ; chr15:g.74417905T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74417905T>G , CM000677.2:g.74417905T>G	GRCh38
NC_000015.9:g.74710246T>G , CM000677.1:g.74710246T>G	GRCh37
NC_000015.8:g.72497299T>G	NCBI36
NG_011733.1:g.21054A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261918.9:c.437A>C MANE Select	ENSP00000261918.4:p.Asn146Thr
ENST00000542748.6:c.-59A>C	ENSP00000441493.1:n.-59A>C
ENST00000261918.8:c.437A>C	ENSP00000261918.4:p.Asn146Thr
ENST00000542748.5:c.-59A>C	ENSP00000441493.1:n.-59A>C
ENST00000543145.6:c.395A>C	ENSP00000438966.2:p.Asn132Thr
ENST00000567345.1:c.-59A>C	ENSP00000454365.1:n.-59A>C
NM_001146029.1:c.395A>C	NP_001139501.1:p.Asn132Thr
NM_001146030.1:c.-59A>C	NP_001139502.1:n.-59A>C
NM_003612.3:c.437A>C	NP_003603.1:p.Asn146Thr
NM_001146029.2:c.395A>C	NP_001139501.1:p.Asn132Thr
NM_001146030.2:c.-59A>C	NP_001139502.1:n.-59A>C
NM_003612.4:c.437A>C	NP_003603.1:p.Asn146Thr
NM_003612.5:c.437A>C MANE Select	NP_003603.1:p.Asn146Thr
NM_001146029.3:c.395A>C	NP_001139501.1:p.Asn132Thr
NM_001146030.3:c.-59A>C	NP_001139502.1:n.-59A>C