Canonical Allele Identifier: CA12483498

Gene: PLXNA4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132504930G>A , CM000669.2:g.132504930G>A	GRCh38
NC_000007.13:g.132189689G>A , CM000669.1:g.132189689G>A	GRCh37
NC_000007.12:g.131840229G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321063.9:c.1188+2576C>T MANE Select	ENSP00000323194.4:n.1188+2576C>T
ENST00000321063.8:c.1188+2576C>T	ENSP00000323194.4:n.1188+2576C>T
ENST00000359827.7:c.1188+2576C>T	ENSP00000352882.3:n.1188+2576C>T
ENST00000378539.5:c.1188+2576C>T	ENSP00000367800.5:n.1188+2576C>T
ENST00000423507.6:c.1188+2576C>T	ENSP00000392772.2:n.1188+2576C>T
NM_001105543.1:c.1188+2576C>T	NP_001099013.1:n.1188+2576C>T
NM_020911.1:c.1188+2576C>T	NP_065962.1:n.1188+2576C>T
NM_181775.3:c.1188+2576C>T	NP_861440.2:n.1188+2576C>T
XM_005250686.3:c.1188+2576C>T	XP_005250743.1:n.1188+2576C>T
XM_005250687.1:c.1188+2576C>T	XP_005250744.1:n.1188+2576C>T
XM_006716171.2:c.1188+2576C>T	XP_006716234.1:n.1188+2576C>T
XM_011516676.1:c.1188+2576C>T	XP_011514978.1:n.1188+2576C>T
XR_927546.1:n.1323+2576C>T
XM_005250686.5:c.1188+2576C>T	XP_005250743.1:n.1188+2576C>T
XM_006716171.4:c.1188+2576C>T	XP_006716234.1:n.1188+2576C>T
XM_011516676.2:c.1188+2576C>T	XP_011514978.1:n.1188+2576C>T
XM_017012779.1:c.1188+2576C>T	XP_016868268.1:n.1188+2576C>T
XR_927546.2:n.1323+2576C>T
NM_001105543.2:c.1188+2576C>T	NP_001099013.1:n.1188+2576C>T
NM_001393897.1:c.1188+2576C>T	NP_001380826.1:n.1188+2576C>T
NM_020911.2:c.1188+2576C>T MANE Select	NP_065962.1:n.1188+2576C>T
NM_181775.4:c.1188+2576C>T	NP_861440.2:n.1188+2576C>T