Canonical Allele Identifier: CA370172667

Gene: PTPRN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.158167219A>T , CM000669.2:g.158167219A>T	GRCh38
NC_000007.13:g.157959911A>T , CM000669.1:g.157959911A>T	GRCh37
NC_000007.12:g.157652672A>T	NCBI36
NG_029966.1:g.425572T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389418.9:c.622T>A MANE Select	ENSP00000374069.4:p.Ser208Thr
ENST00000389413.7:c.622T>A	ENSP00000374064.3:p.Ser208Thr
ENST00000389416.8:c.571T>A	ENSP00000374067.4:p.Ser191Thr
ENST00000389418.8:c.622T>A	ENSP00000374069.4:p.Ser208Thr
ENST00000404321.3:c.349T>A	ENSP00000385464.3:p.Ser117Thr
ENST00000409483.5:c.508T>A	ENSP00000387114.1:p.Ser170Thr
NM_001308267.1:c.508T>A	NP_001295196.1:p.Ser170Thr
NM_001308268.1:c.691T>A	NP_001295197.1:p.Ser231Thr
NM_002847.3:c.622T>A	NP_002838.2:p.Ser208Thr
NM_002847.4:c.622T>A	NP_002838.2:p.Ser208Thr
NM_130842.2:c.571T>A	NP_570857.2:p.Ser191Thr
NM_130842.3:c.571T>A	NP_570857.2:p.Ser191Thr
NM_130843.2:c.622T>A	NP_570858.2:p.Ser208Thr
NM_130843.3:c.622T>A	NP_570858.2:p.Ser208Thr
XM_011516446.1:c.622T>A	XP_011514748.1:p.Ser208Thr
XM_011516447.1:c.622T>A	XP_011514749.1:p.Ser208Thr
XM_011516448.1:c.622T>A	XP_011514750.1:p.Ser208Thr
XM_011516449.1:c.622T>A	XP_011514751.1:p.Ser208Thr
XM_011516447.2:c.622T>A	XP_011514749.1:p.Ser208Thr
XM_011516448.3:c.622T>A	XP_011514750.1:p.Ser208Thr
XM_011516449.2:c.622T>A	XP_011514751.1:p.Ser208Thr
XM_017012475.1:c.424T>A	XP_016867964.1:p.Ser142Thr
XM_017012476.1:c.622T>A	XP_016867965.1:p.Ser208Thr
NM_002847.5:c.622T>A MANE Select	NP_002838.2:p.Ser208Thr
NM_001308267.2:c.508T>A	NP_001295196.1:p.Ser170Thr
NM_130842.4:c.571T>A	NP_570857.2:p.Ser191Thr
NM_130843.4:c.622T>A	NP_570858.2:p.Ser208Thr
NM_001308268.2:c.691T>A	NP_001295197.1:p.Ser231Thr