Canonical Allele Identifier: CA1744049709

Gene: PLXNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.132171497A= , CM000669.2:g.132171497A=	GRCh38
NC_000007.13:g.131856256A= , CM000669.1:g.131856256A=	GRCh37
NC_000007.12:g.131506796A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321063.9:c.4018-2925T= MANE Select	ENSP00000323194.4:n.4018-2925T=
ENST00000321063.8:c.4018-2925T=	ENSP00000323194.4:n.4018-2925T=
ENST00000359827.7:c.4018-2925T=	ENSP00000352882.3:n.4018-2925T=
NM_020911.1:c.4018-2925T=	NP_065962.1:n.4018-2925T=
XM_005250686.3:c.4018-2925T=	XP_005250743.1:n.4018-2925T=
XM_006716171.2:c.4018-2925T=	XP_006716234.1:n.4018-2925T=
XR_927546.1:n.4153-2579T=
XM_005250686.5:c.4018-2925T=	XP_005250743.1:n.4018-2925T=
XM_006716171.4:c.4018-2925T=	XP_006716234.1:n.4018-2925T=
XM_017012779.1:c.3817-2925T=	XP_016868268.1:n.3817-2925T=
XR_927546.2:n.4153-2579T=
NM_001393897.1:c.4018-2925T=	NP_001380826.1:n.4018-2925T=
NM_020911.2:c.4018-2925T= MANE Select	NP_065962.1:n.4018-2925T=