Canonical Allele Identifier: CA1755662891

Gene: PTPRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157594749T= , CM000669.2:g.157594749T=	GRCh38
NC_000007.13:g.157387441T= , CM000669.1:g.157387441T=	GRCh37
NC_000007.12:g.157080202T=	NCBI36
NG_029966.1:g.998042A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002847.5:c.2496+489A= MANE Select	NP_002838.2:n.2496+489A=
ENST00000389418.9:c.2496+489A= MANE Select	ENSP00000374069.4:n.2496+489A=
NM_001308267.1:c.2382+489A=	NP_001295196.1:n.2382+489A=
NM_001308267.2:c.2382+489A=	NP_001295196.1:n.2382+489A=
NM_001308268.1:c.2565+489A=	NP_001295197.1:n.2565+489A=
NM_001308268.2:c.2565+489A=	NP_001295197.1:n.2565+489A=
NM_002847.3:c.2496+489A=	NP_002838.2:n.2496+489A=
NM_002847.4:c.2496+489A=	NP_002838.2:n.2496+489A=
NM_130842.2:c.2445+489A=	NP_570857.2:n.2445+489A=
NM_130842.3:c.2445+489A=	NP_570857.2:n.2445+489A=
NM_130842.4:c.2445+489A=	NP_570857.2:n.2445+489A=
NM_130843.2:c.2409+489A=	NP_570858.2:n.2409+489A=
NM_130843.3:c.2409+489A=	NP_570858.2:n.2409+489A=
NM_130843.4:c.2409+489A=	NP_570858.2:n.2409+489A=
ENST00000389413.7:c.2409+489A=	ENSP00000374064.3:n.2409+489A=
ENST00000389416.8:c.2445+489A=	ENSP00000374067.4:n.2445+489A=
ENST00000389418.8:c.2496+489A=	ENSP00000374069.4:n.2496+489A=
ENST00000409483.5:c.2382+489A=	ENSP00000387114.1:n.2382+489A=
ENST00000648371.1:c.300+489A=	ENSP00000498058.1:n.300+489A=
XM_011516446.1:c.*86A=	XP_011514748.1:n.*86A=
XM_017012475.1:c.2298+489A=	XP_016867964.1:n.2298+489A=
XM_017012476.1:c.*36A=	XP_016867965.1:n.*36A=