Canonical Allele Identifier: CA4390089

Gene: ZAN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100750838G>A , CM000669.2:g.100750838G>A	GRCh38
NC_000007.13:g.100348461G>A , CM000669.1:g.100348461G>A	GRCh37
NC_000007.12:g.100186397G>A	NCBI36
NG_029544.2:g.22213G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003386.3:c.1463G>A MANE Select	NP_003377.2:p.Arg488His
ENST00000613979.5:c.1463G>A MANE Select	ENSP00000480750.1:p.Arg488His
NM_003386.2:c.1463G>A	NP_003377.2:p.Arg488His
NM_173059.2:c.1463G>A	NP_775082.2:p.Arg488His
NM_173059.3:c.1463G>A	NP_775082.2:p.Arg488His
NR_111917.1:n.1628G>A
NR_111917.2:n.1659G>A
NR_111918.1:n.1628G>A
NR_111918.2:n.1659G>A
NR_111919.1:n.1628G>A
NR_111919.2:n.1659G>A
ENST00000538115.5:c.1463G>A	ENSP00000445091.2:p.Arg488His
ENST00000542585.5:c.1463G>A	ENSP00000444427.2:p.Arg488His
ENST00000546213.5:c.1463G>A	ENSP00000441117.2:p.Arg488His
ENST00000546292.2:c.1463G>A	ENSP00000445943.2:p.Arg488His
ENST00000613979.4:c.1463G>A	ENSP00000480750.1:p.Arg488His
ENST00000618565.4:c.1463G>A	ENSP00000478371.1:p.Arg488His
ENST00000620596.4:c.1463G>A	ENSP00000481742.1:p.Arg488His
ENST00000620868.4:n.1628G>A
XM_011516555.1:c.1463G>A	XP_011514857.1:p.Arg488His
XM_011516555.2:c.1463G>A	XP_011514857.1:p.Arg488His