Canonical Allele Identifier: CA1744042288

Gene: PLXNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132130584G= , CM000669.2:g.132130584G=	GRCh38
NC_000007.13:g.131815343G= , CM000669.1:g.131815343G=	GRCh37
NC_000007.12:g.131465883G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020911.2:c.5590-10C= MANE Select	NP_065962.1:n.5590-10C=
ENST00000321063.9:c.5590-10C= MANE Select	ENSP00000323194.4:n.5590-10C=
NM_001393897.1:c.5590-10C=	NP_001380826.1:n.5590-10C=
NM_020911.1:c.5590-10C=	NP_065962.1:n.5590-10C=
ENST00000321063.8:c.5590-10C=	ENSP00000323194.4:n.5590-10C=
ENST00000359827.7:c.5590-10C=	ENSP00000352882.3:n.5590-10C=
XM_005250686.3:c.5590-10C=	XP_005250743.1:n.5590-10C=
XM_005250686.5:c.5590-10C=	XP_005250743.1:n.5590-10C=
XM_006716171.2:c.5590-10C=	XP_006716234.1:n.5590-10C=
XM_006716171.4:c.5590-10C=	XP_006716234.1:n.5590-10C=
XM_017012779.1:c.5389-10C=	XP_016868268.1:n.5389-10C=