Canonical Allele Identifier: CA2838373341

Gene: PTPRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157785464C>A , CM000669.2:g.157785464C>A	GRCh38
NC_000007.13:g.157578156C>A , CM000669.1:g.157578156C>A	GRCh37
NC_000007.12:g.157270917C>A	NCBI36
NG_029966.1:g.807327G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389418.9:c.1789-102527G>T MANE Select	ENSP00000374069.4:n.1789-102527G>T
ENST00000389413.7:c.1702-102527G>T	ENSP00000374064.3:n.1702-102527G>T
ENST00000389416.8:c.1738-102527G>T	ENSP00000374067.4:n.1738-102527G>T
ENST00000389418.8:c.1789-102527G>T	ENSP00000374069.4:n.1789-102527G>T
ENST00000409483.5:c.1675-102527G>T	ENSP00000387114.1:n.1675-102527G>T
NM_001308267.1:c.1675-102527G>T	NP_001295196.1:n.1675-102527G>T
NM_001308268.1:c.1858-102527G>T	NP_001295197.1:n.1858-102527G>T
NM_002847.3:c.1789-102527G>T	NP_002838.2:n.1789-102527G>T
NM_002847.4:c.1789-102527G>T	NP_002838.2:n.1789-102527G>T
NM_130842.2:c.1738-102527G>T	NP_570857.2:n.1738-102527G>T
NM_130842.3:c.1738-102527G>T	NP_570857.2:n.1738-102527G>T
NM_130843.2:c.1702-102527G>T	NP_570858.2:n.1702-102527G>T
NM_130843.3:c.1702-102527G>T	NP_570858.2:n.1702-102527G>T
XM_011516446.1:c.1789-102527G>T	XP_011514748.1:n.1789-102527G>T
XM_017012475.1:c.1591-102527G>T	XP_016867964.1:n.1591-102527G>T
XM_017012476.1:c.1789-102527G>T	XP_016867965.1:n.1789-102527G>T
NM_002847.5:c.1789-102527G>T MANE Select	NP_002838.2:n.1789-102527G>T
NM_001308267.2:c.1675-102527G>T	NP_001295196.1:n.1675-102527G>T
NM_130842.4:c.1738-102527G>T	NP_570857.2:n.1738-102527G>T
NM_130843.4:c.1702-102527G>T	NP_570858.2:n.1702-102527G>T
NM_001308268.2:c.1858-102527G>T	NP_001295197.1:n.1858-102527G>T