Canonical Allele Identifier: CA457679847

Gene: PLXNA4

Linked Data

• dbSNP Id: rs13232207
• gnomAD v3: 7-132174919-G-A
• gnomAD v4: 7-132174919-G-A
• MyVariant Identifiers: chr7:g.131859678G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132174919G>A , CM000669.2:g.132174919G>A	GRCh38
NC_000007.13:g.131859678G>A , CM000669.1:g.131859678G>A	GRCh37
NC_000007.12:g.131510218G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321063.9:c.3876C>T MANE Select	ENSP00000323194.4:p.Ala1292=
ENST00000321063.8:c.3876C>T	ENSP00000323194.4:p.Ala1292=
ENST00000359827.7:c.3876C>T	ENSP00000352882.3:p.Ala1292=
NM_020911.1:c.3876C>T	NP_065962.1:p.Ala1292=
XM_005250686.3:c.3876C>T	XP_005250743.1:p.Ala1292=
XM_006716171.2:c.3876C>T	XP_006716234.1:p.Ala1292=
XM_011516676.1:c.3876C>T	XP_011514978.1:p.Ala1292=
XR_927546.1:n.4011C>T
XM_005250686.5:c.3876C>T	XP_005250743.1:p.Ala1292=
XM_006716171.4:c.3876C>T	XP_006716234.1:p.Ala1292=
XM_011516676.2:c.3876C>T	XP_011514978.1:p.Ala1292=
XM_017012779.1:c.3675C>T	XP_016868268.1:p.Ala1225=
XR_927546.2:n.4011C>T
NM_001393897.1:c.3876C>T	NP_001380826.1:p.Ala1292=
NM_020911.2:c.3876C>T MANE Select	NP_065962.1:p.Ala1292=