Canonical Allele Identifier: CA457837397

Gene: PLXNA4

Linked Data

• MyVariant Identifiers: chr7:g.132029997C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132345238C>T , CM000669.2:g.132345238C>T	GRCh38
NC_000007.13:g.132029997C>T , CM000669.1:g.132029997C>T	GRCh37
NC_000007.12:g.131680537C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321063.9:c.1372-47016G>A MANE Select	ENSP00000323194.4:n.1372-47016G>A
ENST00000321063.8:c.1372-47016G>A	ENSP00000323194.4:n.1372-47016G>A
ENST00000359827.7:c.1372-47016G>A	ENSP00000352882.3:n.1372-47016G>A
NM_020911.1:c.1372-47016G>A	NP_065962.1:n.1372-47016G>A
XM_005250686.3:c.1372-47016G>A	XP_005250743.1:n.1372-47016G>A
XM_006716171.2:c.1372-47016G>A	XP_006716234.1:n.1372-47016G>A
XM_011516676.1:c.1372-47016G>A	XP_011514978.1:n.1372-47016G>A
XR_927546.1:n.1507-47016G>A
XM_005250686.5:c.1372-47016G>A	XP_005250743.1:n.1372-47016G>A
XM_006716171.4:c.1372-47016G>A	XP_006716234.1:n.1372-47016G>A
XM_011516676.2:c.1372-47016G>A	XP_011514978.1:n.1372-47016G>A
XM_017012779.1:c.1372-47016G>A	XP_016868268.1:n.1372-47016G>A
XR_927546.2:n.1507-47016G>A
NM_001393897.1:c.1372-47016G>A	NP_001380826.1:n.1372-47016G>A
NM_020911.2:c.1372-47016G>A MANE Select	NP_065962.1:n.1372-47016G>A