Canonical Allele Identifier: CA578023937

Gene: PLXNA4

Linked Data

• dbSNP Id: rs1474927976
• gnomAD v2: 7-132029956-T-TAAC
• gnomAD v3: 7-132345197-T-TAAC
• gnomAD v4: 7-132345197-T-TAAC
• MyVariant Identifiers: chr7:g.132029956_132029957insAAC (hg19) ; chr7:g.132345197_132345198insAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132345198_132345199insACA , CM000669.2:g.132345198_132345199insACA	GRCh38
NC_000007.13:g.132029957_132029958insACA , CM000669.1:g.132029957_132029958insACA	GRCh37
NC_000007.12:g.131680497_131680498insACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321063.9:c.1372-46976_1372-46975insGTT MANE Select	ENSP00000323194.4:n.1372-46976_1372-46975insGTT
ENST00000321063.8:c.1372-46976_1372-46975insGTT	ENSP00000323194.4:n.1372-46976_1372-46975insGTT
ENST00000359827.7:c.1372-46976_1372-46975insGTT	ENSP00000352882.3:n.1372-46976_1372-46975insGTT
NM_020911.1:c.1372-46976_1372-46975insGTT	NP_065962.1:n.1372-46976_1372-46975insGTT
XM_005250686.3:c.1372-46976_1372-46975insGTT	XP_005250743.1:n.1372-46976_1372-46975insGTT
XM_006716171.2:c.1372-46976_1372-46975insGTT	XP_006716234.1:n.1372-46976_1372-46975insGTT
XM_011516676.1:c.1372-46976_1372-46975insGTT	XP_011514978.1:n.1372-46976_1372-46975insGTT
XR_927546.1:n.1507-46976_1507-46975insGTT
XM_005250686.5:c.1372-46976_1372-46975insGTT	XP_005250743.1:n.1372-46976_1372-46975insGTT
XM_006716171.4:c.1372-46976_1372-46975insGTT	XP_006716234.1:n.1372-46976_1372-46975insGTT
XM_011516676.2:c.1372-46976_1372-46975insGTT	XP_011514978.1:n.1372-46976_1372-46975insGTT
XM_017012779.1:c.1372-46976_1372-46975insGTT	XP_016868268.1:n.1372-46976_1372-46975insGTT
XR_927546.2:n.1507-46976_1507-46975insGTT
NM_001393897.1:c.1372-46976_1372-46975insGTT	NP_001380826.1:n.1372-46976_1372-46975insGTT
NM_020911.2:c.1372-46976_1372-46975insGTT MANE Select	NP_065962.1:n.1372-46976_1372-46975insGTT