Canonical Allele Identifier: CA2285433094

Gene: PTPN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12836119_12836120delinsCT , CM000680.2:g.12836119_12836120delinsCT	GRCh38
NC_000018.9:g.12836118_12836119delinsCT , CM000680.1:g.12836118_12836119delinsCT	GRCh37
NC_000018.8:g.12826118_12826119delinsCT	NCBI36
NG_029116.1:g.53216_53217delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309660.10:c.261+671_261+672delinsAG MANE Select	ENSP00000311857.3:n.261+671_261+672delinsAG
ENST00000645191.1:c.-37+671_-37+672delinsAG	ENSP00000493693.1:n.-37+671_-37+672delinsAG
ENST00000645816.1:c.261+671_261+672delinsAG	ENSP00000494336.1:n.261+671_261+672delinsAG
ENST00000646492.1:c.-37+671_-37+672delinsAG	ENSP00000496181.1:n.-37+671_-37+672delinsAG
ENST00000309660.9:c.261+671_261+672delinsAG	ENSP00000311857.3:n.261+671_261+672delinsAG
ENST00000327283.7:c.261+671_261+672delinsAG	ENSP00000320298.3:n.261+671_261+672delinsAG
ENST00000353319.8:c.261+671_261+672delinsAG	ENSP00000320546.3:n.261+671_261+672delinsAG
ENST00000587703.5:c.34+671_34+672delinsAG
ENST00000589216.1:c.*41+671_*41+672delinsAG	ENSP00000468408.1:n.*41+671_*41+672delinsAG
ENST00000591115.5:c.261+671_261+672delinsAG	ENSP00000466936.1:n.261+671_261+672delinsAG
ENST00000591305.5:c.*41+671_*41+672delinsAG	ENSP00000468012.1:n.*41+671_*41+672delinsAG
ENST00000591497.5:c.174+671_174+672delinsAG	ENSP00000467823.1:n.174+671_174+672delinsAG
ENST00000592059.5:c.-37+671_-37+672delinsAG	ENSP00000466206.1:n.-37+671_-37+672delinsAG
ENST00000592776.1:c.261+671_261+672delinsAG	ENSP00000468155.1:n.261+671_261+672delinsAG
NM_001207013.1:c.261+671_261+672delinsAG	NP_001193942.1:n.261+671_261+672delinsAG
NM_001308287.1:c.174+671_174+672delinsAG	NP_001295216.1:n.174+671_174+672delinsAG
NM_002828.3:c.261+671_261+672delinsAG	NP_002819.2:n.261+671_261+672delinsAG
NM_080422.2:c.261+671_261+672delinsAG	NP_536347.1:n.261+671_261+672delinsAG
NM_080423.2:c.261+671_261+672delinsAG	NP_536348.1:n.261+671_261+672delinsAG
XM_005258124.2:c.261+671_261+672delinsAG	XP_005258181.1:n.261+671_261+672delinsAG
XM_005258125.2:c.261+671_261+672delinsAG	XP_005258182.1:n.261+671_261+672delinsAG
XM_011525705.1:c.174+671_174+672delinsAG	XP_011524007.1:n.174+671_174+672delinsAG
XM_011525706.1:c.261+671_261+672delinsAG	XP_011524008.1:n.261+671_261+672delinsAG
XM_005258124.4:c.261+671_261+672delinsAG	XP_005258181.1:n.261+671_261+672delinsAG
XM_005258125.4:c.261+671_261+672delinsAG	XP_005258182.1:n.261+671_261+672delinsAG
XM_011525705.3:c.174+671_174+672delinsAG	XP_011524007.1:n.174+671_174+672delinsAG
XM_011525706.2:c.261+671_261+672delinsAG	XP_011524008.1:n.261+671_261+672delinsAG
XM_017025884.1:c.261+671_261+672delinsAG	XP_016881373.1:n.261+671_261+672delinsAG
XM_017025885.2:c.174+671_174+672delinsAG	XP_016881374.1:n.174+671_174+672delinsAG
XM_017025886.1:c.-37+671_-37+672delinsAG	XP_016881375.1:n.-37+671_-37+672delinsAG
XM_017025887.2:c.-37+671_-37+672delinsAG	XP_016881376.1:n.-37+671_-37+672delinsAG
XM_017025888.2:c.-37+671_-37+672delinsAG	XP_016881377.1:n.-37+671_-37+672delinsAG
XM_024451228.1:c.261+671_261+672delinsAG	XP_024306996.1:n.261+671_261+672delinsAG
XM_024451229.1:c.-37+671_-37+672delinsAG	XP_024306997.1:n.-37+671_-37+672delinsAG
XM_024451230.1:c.-37+671_-37+672delinsAG	XP_024306998.1:n.-37+671_-37+672delinsAG
NM_002828.4:c.261+671_261+672delinsAG MANE Select	NP_002819.2:n.261+671_261+672delinsAG
NM_001207013.2:c.261+671_261+672delinsAG	NP_001193942.1:n.261+671_261+672delinsAG
NM_080422.3:c.261+671_261+672delinsAG	NP_536347.1:n.261+671_261+672delinsAG
NM_080423.3:c.261+671_261+672delinsAG	NP_536348.1:n.261+671_261+672delinsAG