Canonical Allele Identifier: CA1107322402

Gene: PLXNA4

Linked Data

• dbSNP Id: rs1803199750
• gnomAD v3: 7-132345234-A-AAG
• gnomAD v4: 7-132345234-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132345234_132345235insAG , CM000669.2:g.132345234_132345235insAG	GRCh38
NC_000007.13:g.132029993_132029994insAG , CM000669.1:g.132029993_132029994insAG	GRCh37
NC_000007.12:g.131680533_131680534insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321063.9:c.1372-47013_1372-47012insCT MANE Select	ENSP00000323194.4:n.1372-47013_1372-47012insCT
ENST00000321063.8:c.1372-47013_1372-47012insCT	ENSP00000323194.4:n.1372-47013_1372-47012insCT
ENST00000359827.7:c.1372-47013_1372-47012insCT	ENSP00000352882.3:n.1372-47013_1372-47012insCT
NM_020911.1:c.1372-47013_1372-47012insCT	NP_065962.1:n.1372-47013_1372-47012insCT
XM_005250686.3:c.1372-47013_1372-47012insCT	XP_005250743.1:n.1372-47013_1372-47012insCT
XM_006716171.2:c.1372-47013_1372-47012insCT	XP_006716234.1:n.1372-47013_1372-47012insCT
XM_011516676.1:c.1372-47013_1372-47012insCT	XP_011514978.1:n.1372-47013_1372-47012insCT
XR_927546.1:n.1507-47013_1507-47012insCT
XM_005250686.5:c.1372-47013_1372-47012insCT	XP_005250743.1:n.1372-47013_1372-47012insCT
XM_006716171.4:c.1372-47013_1372-47012insCT	XP_006716234.1:n.1372-47013_1372-47012insCT
XM_011516676.2:c.1372-47013_1372-47012insCT	XP_011514978.1:n.1372-47013_1372-47012insCT
XM_017012779.1:c.1372-47013_1372-47012insCT	XP_016868268.1:n.1372-47013_1372-47012insCT
XR_927546.2:n.1507-47013_1507-47012insCT
NM_001393897.1:c.1372-47013_1372-47012insCT	NP_001380826.1:n.1372-47013_1372-47012insCT
NM_020911.2:c.1372-47013_1372-47012insCT MANE Select	NP_065962.1:n.1372-47013_1372-47012insCT