Canonical Allele Identifier: CA1744049671

Gene: PLXNA4

Linked Data

• dbSNP Id: rs1796283834

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132171461G>A , CM000669.2:g.132171461G>A	GRCh38
NC_000007.13:g.131856220G>A , CM000669.1:g.131856220G>A	GRCh37
NC_000007.12:g.131506760G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321063.9:c.4018-2889C>T MANE Select	ENSP00000323194.4:n.4018-2889C>T
ENST00000321063.8:c.4018-2889C>T	ENSP00000323194.4:n.4018-2889C>T
ENST00000359827.7:c.4018-2889C>T	ENSP00000352882.3:n.4018-2889C>T
NM_020911.1:c.4018-2889C>T	NP_065962.1:n.4018-2889C>T
XM_005250686.3:c.4018-2889C>T	XP_005250743.1:n.4018-2889C>T
XM_006716171.2:c.4018-2889C>T	XP_006716234.1:n.4018-2889C>T
XR_927546.1:n.4153-2543C>T
XM_005250686.5:c.4018-2889C>T	XP_005250743.1:n.4018-2889C>T
XM_006716171.4:c.4018-2889C>T	XP_006716234.1:n.4018-2889C>T
XM_017012779.1:c.3817-2889C>T	XP_016868268.1:n.3817-2889C>T
XR_927546.2:n.4153-2543C>T
NM_001393897.1:c.4018-2889C>T	NP_001380826.1:n.4018-2889C>T
NM_020911.2:c.4018-2889C>T MANE Select	NP_065962.1:n.4018-2889C>T