Canonical Allele Identifier: CA1755984990

Gene: PTPRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.158192457C= , CM000669.2:g.158192457C=	GRCh38
NC_000007.13:g.157985149C= , CM000669.1:g.157985149C=	GRCh37
NC_000007.12:g.157677910C=	NCBI36
NG_029966.1:g.400334G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389418.9:c.419G= MANE Select	ENSP00000374069.4:p.Ser140=
ENST00000389413.7:c.419G=	ENSP00000374064.3:p.Ser140=
ENST00000389416.8:c.368G=	ENSP00000374067.4:p.Ser123=
ENST00000389418.8:c.419G=	ENSP00000374069.4:p.Ser140=
ENST00000404321.3:c.146G=	ENSP00000385464.3:p.Ser49=
ENST00000409483.5:c.305G=	ENSP00000387114.1:p.Ser102=
NM_001308267.1:c.305G=	NP_001295196.1:p.Ser102=
NM_001308268.1:c.488G=	NP_001295197.1:p.Ser163=
NM_002847.3:c.419G=	NP_002838.2:p.Ser140=
NM_002847.4:c.419G=	NP_002838.2:p.Ser140=
NM_130842.2:c.368G=	NP_570857.2:p.Ser123=
NM_130842.3:c.368G=	NP_570857.2:p.Ser123=
NM_130843.2:c.419G=	NP_570858.2:p.Ser140=
NM_130843.3:c.419G=	NP_570858.2:p.Ser140=
XM_011516446.1:c.419G=	XP_011514748.1:p.Ser140=
XM_011516447.1:c.419G=	XP_011514749.1:p.Ser140=
XM_011516448.1:c.419G=	XP_011514750.1:p.Ser140=
XM_011516449.1:c.419G=	XP_011514751.1:p.Ser140=
XM_011516447.2:c.419G=	XP_011514749.1:p.Ser140=
XM_011516448.3:c.419G=	XP_011514750.1:p.Ser140=
XM_011516449.2:c.419G=	XP_011514751.1:p.Ser140=
XM_017012475.1:c.221G=	XP_016867964.1:p.Ser74=
XM_017012476.1:c.419G=	XP_016867965.1:p.Ser140=
NM_002847.5:c.419G= MANE Select	NP_002838.2:p.Ser140=
NM_001308267.2:c.305G=	NP_001295196.1:p.Ser102=
NM_130842.4:c.368G=	NP_570857.2:p.Ser123=
NM_130843.4:c.419G=	NP_570858.2:p.Ser140=
NM_001308268.2:c.488G=	NP_001295197.1:p.Ser163=