Canonical Allele Identifier: CA1756122560

Gene: PTPRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.158430414A= , CM000669.2:g.158430414A=	GRCh38
NC_000007.13:g.158223106A= , CM000669.1:g.158223106A=	GRCh37
NC_000007.12:g.157915867A=	NCBI36
NG_029966.1:g.162377T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389418.9:c.163+59321T= MANE Select	ENSP00000374069.4:n.163+59321T=
ENST00000389413.7:c.163+59321T=	ENSP00000374064.3:n.163+59321T=
ENST00000389416.8:c.113-113482T=	ENSP00000374067.4:n.113-113482T=
ENST00000389418.8:c.163+59321T=	ENSP00000374069.4:n.163+59321T=
ENST00000409483.5:c.163+59321T=	ENSP00000387114.1:n.163+59321T=
NM_001308267.1:c.163+59321T=	NP_001295196.1:n.163+59321T=
NM_001308268.1:c.232+59321T=	NP_001295197.1:n.232+59321T=
NM_002847.3:c.163+59321T=	NP_002838.2:n.163+59321T=
NM_002847.4:c.163+59321T=	NP_002838.2:n.163+59321T=
NM_130842.2:c.113-113482T=	NP_570857.2:n.113-113482T=
NM_130842.3:c.113-113482T=	NP_570857.2:n.113-113482T=
NM_130843.2:c.163+59321T=	NP_570858.2:n.163+59321T=
NM_130843.3:c.163+59321T=	NP_570858.2:n.163+59321T=
XM_011516446.1:c.163+59321T=	XP_011514748.1:n.163+59321T=
XM_011516447.1:c.163+59321T=	XP_011514749.1:n.163+59321T=
XM_011516448.1:c.163+59321T=	XP_011514750.1:n.163+59321T=
XM_011516449.1:c.163+59321T=	XP_011514751.1:n.163+59321T=
XM_011516447.2:c.163+59321T=	XP_011514749.1:n.163+59321T=
XM_011516448.3:c.163+59321T=	XP_011514750.1:n.163+59321T=
XM_011516449.2:c.163+59321T=	XP_011514751.1:n.163+59321T=
XM_017012476.1:c.163+59321T=	XP_016867965.1:n.163+59321T=
NM_002847.5:c.163+59321T= MANE Select	NP_002838.2:n.163+59321T=
NM_001308267.2:c.163+59321T=	NP_001295196.1:n.163+59321T=
NM_130842.4:c.113-113482T=	NP_570857.2:n.113-113482T=
NM_130843.4:c.163+59321T=	NP_570858.2:n.163+59321T=
NM_001308268.2:c.232+59321T=	NP_001295197.1:n.232+59321T=