Canonical Allele Identifier: CA12528199
Gene: PTPRN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.158344294A>T , CM000669.2:g.158344294A>T GRCh38
NC_000007.13:g.158136986A>T , CM000669.1:g.158136986A>T GRCh37
NC_000007.12:g.157829747A>T NCBI36
NG_029966.1:g.248497T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389418.9:c.164-27362T>A MANE Select ENSP00000374069.4:n.164-27362T>A
ENST00000389413.7:c.164-27362T>A ENSP00000374064.3:n.164-27362T>A
ENST00000389416.8:c.113-27362T>A ENSP00000374067.4:n.113-27362T>A
ENST00000389418.8:c.164-27362T>A ENSP00000374069.4:n.164-27362T>A
ENST00000409483.5:c.164-139021T>A ENSP00000387114.1:n.164-139021T>A
NM_001308267.1:c.164-139021T>A NP_001295196.1:n.164-139021T>A
NM_001308268.1:c.233-27362T>A NP_001295197.1:n.233-27362T>A
NM_002847.3:c.164-27362T>A NP_002838.2:n.164-27362T>A
NM_002847.4:c.164-27362T>A NP_002838.2:n.164-27362T>A
NM_130842.2:c.113-27362T>A NP_570857.2:n.113-27362T>A
NM_130842.3:c.113-27362T>A NP_570857.2:n.113-27362T>A
NM_130843.2:c.164-27362T>A NP_570858.2:n.164-27362T>A
NM_130843.3:c.164-27362T>A NP_570858.2:n.164-27362T>A
XM_011516446.1:c.164-27362T>A XP_011514748.1:n.164-27362T>A
XM_011516447.1:c.164-27362T>A XP_011514749.1:n.164-27362T>A
XM_011516448.1:c.164-27362T>A XP_011514750.1:n.164-27362T>A
XM_011516449.1:c.164-27362T>A XP_011514751.1:n.164-27362T>A
XM_011516447.2:c.164-27362T>A XP_011514749.1:n.164-27362T>A
XM_011516448.3:c.164-27362T>A XP_011514750.1:n.164-27362T>A
XM_011516449.2:c.164-27362T>A XP_011514751.1:n.164-27362T>A
XM_017012476.1:c.164-27362T>A XP_016867965.1:n.164-27362T>A
NM_002847.5:c.164-27362T>A MANE Select NP_002838.2:n.164-27362T>A
NM_001308267.2:c.164-139021T>A NP_001295196.1:n.164-139021T>A
NM_130842.4:c.113-27362T>A NP_570857.2:n.113-27362T>A
NM_130843.4:c.164-27362T>A NP_570858.2:n.164-27362T>A
NM_001308268.2:c.233-27362T>A NP_001295197.1:n.233-27362T>A
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