Canonical Allele Identifier: CA2777944015
Gene: PLXNA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.132171477C>T , CM000669.2:g.132171477C>T GRCh38
NC_000007.13:g.131856236C>T , CM000669.1:g.131856236C>T GRCh37
NC_000007.12:g.131506776C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321063.9:c.4018-2905G>A MANE Select ENSP00000323194.4:n.4018-2905G>A
ENST00000321063.8:c.4018-2905G>A ENSP00000323194.4:n.4018-2905G>A
ENST00000359827.7:c.4018-2905G>A ENSP00000352882.3:n.4018-2905G>A
NM_020911.1:c.4018-2905G>A NP_065962.1:n.4018-2905G>A
XM_005250686.3:c.4018-2905G>A XP_005250743.1:n.4018-2905G>A
XM_006716171.2:c.4018-2905G>A XP_006716234.1:n.4018-2905G>A
XR_927546.1:n.4153-2559G>A
XM_005250686.5:c.4018-2905G>A XP_005250743.1:n.4018-2905G>A
XM_006716171.4:c.4018-2905G>A XP_006716234.1:n.4018-2905G>A
XM_017012779.1:c.3817-2905G>A XP_016868268.1:n.3817-2905G>A
XR_927546.2:n.4153-2559G>A
NM_001393897.1:c.4018-2905G>A NP_001380826.1:n.4018-2905G>A
NM_020911.2:c.4018-2905G>A MANE Select NP_065962.1:n.4018-2905G>A
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