Canonical Allele Identifier: CA456144980

Gene: SEMA3A

Linked Data

• MyVariant Identifiers: chr7:g.83610762A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981446A>C , CM000669.2:g.83981446A>C	GRCh38
NC_000007.13:g.83610762A>C , CM000669.1:g.83610762A>C	GRCh37
NC_000007.12:g.83448698A>C	NCBI36
NG_011489.1:g.218456T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265362.9:c.1527T>G MANE Select	ENSP00000265362.3:p.Val509=
ENST00000265362.8:c.1527T>G	ENSP00000265362.3:p.Val509=
ENST00000436949.5:c.1527T>G	ENSP00000415260.1:p.Val509=
NM_006080.2:c.1527T>G	NP_006071.1:p.Val509=
XM_005250110.2:c.1527T>G	XP_005250167.1:p.Val509=
XM_005250111.3:c.1527T>G	XP_005250168.1:p.Val509=
XM_006715839.2:c.1527T>G	XP_006715902.1:p.Val509=
XM_011515734.1:c.1527T>G	XP_011514036.1:p.Val509=
XM_011515735.1:c.1527T>G	XP_011514037.1:p.Val509=
XM_005250110.3:c.1527T>G	XP_005250167.1:p.Val509=
XM_005250111.4:c.1527T>G	XP_005250168.1:p.Val509=
XM_006715839.3:c.1527T>G	XP_006715902.1:p.Val509=
XM_011515734.3:c.1527T>G	XP_011514036.1:p.Val509=
XM_017011673.1:c.1527T>G	XP_016867162.1:p.Val509=
XM_024446633.1:c.1527T>G	XP_024302401.1:p.Val509=
NM_006080.3:c.1527T>G MANE Select	NP_006071.1:p.Val509=