Canonical Allele Identifier: CA1755945047

Gene: PTPRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.158167203C= , CM000669.2:g.158167203C=	GRCh38
NC_000007.13:g.157959895C= , CM000669.1:g.157959895C=	GRCh37
NC_000007.12:g.157652656C=	NCBI36
NG_029966.1:g.425588G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389418.9:c.638G= MANE Select	ENSP00000374069.4:p.Arg213=
ENST00000389413.7:c.638G=	ENSP00000374064.3:p.Arg213=
ENST00000389416.8:c.587G=	ENSP00000374067.4:p.Arg196=
ENST00000389418.8:c.638G=	ENSP00000374069.4:p.Arg213=
ENST00000404321.3:c.365G=	ENSP00000385464.3:p.Arg122=
ENST00000409483.5:c.524G=	ENSP00000387114.1:p.Arg175=
NM_001308267.1:c.524G=	NP_001295196.1:p.Arg175=
NM_001308268.1:c.707G=	NP_001295197.1:p.Arg236=
NM_002847.3:c.638G=	NP_002838.2:p.Arg213=
NM_002847.4:c.638G=	NP_002838.2:p.Arg213=
NM_130842.2:c.587G=	NP_570857.2:p.Arg196=
NM_130842.3:c.587G=	NP_570857.2:p.Arg196=
NM_130843.2:c.638G=	NP_570858.2:p.Arg213=
NM_130843.3:c.638G=	NP_570858.2:p.Arg213=
XM_011516446.1:c.638G=	XP_011514748.1:p.Arg213=
XM_011516447.1:c.638G=	XP_011514749.1:p.Arg213=
XM_011516448.1:c.638G=	XP_011514750.1:p.Arg213=
XM_011516449.1:c.638G=	XP_011514751.1:p.Arg213=
XM_011516447.2:c.638G=	XP_011514749.1:p.Arg213=
XM_011516448.3:c.638G=	XP_011514750.1:p.Arg213=
XM_011516449.2:c.638G=	XP_011514751.1:p.Arg213=
XM_017012475.1:c.440G=	XP_016867964.1:p.Arg147=
XM_017012476.1:c.638G=	XP_016867965.1:p.Arg213=
NM_002847.5:c.638G= MANE Select	NP_002838.2:p.Arg213=
NM_001308267.2:c.524G=	NP_001295196.1:p.Arg175=
NM_130842.4:c.587G=	NP_570857.2:p.Arg196=
NM_130843.4:c.638G=	NP_570858.2:p.Arg213=
NM_001308268.2:c.707G=	NP_001295197.1:p.Arg236=