Canonical Allele Identifier: CA12639193

Gene: PLXNA4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132144369C>T , CM000669.2:g.132144369C>T	GRCh38
NC_000007.13:g.131829128C>T , CM000669.1:g.131829128C>T	GRCh37
NC_000007.12:g.131479668C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321063.9:c.5225+750G>A MANE Select	ENSP00000323194.4:n.5225+750G>A
ENST00000321063.8:c.5225+750G>A	ENSP00000323194.4:n.5225+750G>A
ENST00000359827.7:c.5225+750G>A	ENSP00000352882.3:n.5225+750G>A
ENST00000496550.1:n.389+750G>A
NM_020911.1:c.5225+750G>A	NP_065962.1:n.5225+750G>A
XM_005250686.3:c.5225+750G>A	XP_005250743.1:n.5225+750G>A
XM_006716171.2:c.5225+750G>A	XP_006716234.1:n.5225+750G>A
XM_005250686.5:c.5225+750G>A	XP_005250743.1:n.5225+750G>A
XM_006716171.4:c.5225+750G>A	XP_006716234.1:n.5225+750G>A
XM_017012779.1:c.5024+750G>A	XP_016868268.1:n.5024+750G>A
NM_001393897.1:c.5225+750G>A	NP_001380826.1:n.5225+750G>A
NM_020911.2:c.5225+750G>A MANE Select	NP_065962.1:n.5225+750G>A