Canonical Allele Identifier: CA1744162753

Gene: PLXNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132345086G= , CM000669.2:g.132345086G=	GRCh38
NC_000007.13:g.132029845G= , CM000669.1:g.132029845G=	GRCh37
NC_000007.12:g.131680385G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321063.9:c.1372-46864C= MANE Select	ENSP00000323194.4:n.1372-46864C=
ENST00000321063.8:c.1372-46864C=	ENSP00000323194.4:n.1372-46864C=
ENST00000359827.7:c.1372-46864C=	ENSP00000352882.3:n.1372-46864C=
NM_020911.1:c.1372-46864C=	NP_065962.1:n.1372-46864C=
XM_005250686.3:c.1372-46864C=	XP_005250743.1:n.1372-46864C=
XM_006716171.2:c.1372-46864C=	XP_006716234.1:n.1372-46864C=
XM_011516676.1:c.1372-46864C=	XP_011514978.1:n.1372-46864C=
XR_927546.1:n.1507-46864C=
XM_005250686.5:c.1372-46864C=	XP_005250743.1:n.1372-46864C=
XM_006716171.4:c.1372-46864C=	XP_006716234.1:n.1372-46864C=
XM_011516676.2:c.1372-46864C=	XP_011514978.1:n.1372-46864C=
XM_017012779.1:c.1372-46864C=	XP_016868268.1:n.1372-46864C=
XR_927546.2:n.1507-46864C=
NM_001393897.1:c.1372-46864C=	NP_001380826.1:n.1372-46864C=
NM_020911.2:c.1372-46864C= MANE Select	NP_065962.1:n.1372-46864C=