Canonical Allele Identifier: CA2285433035

Gene: PTPN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12835990_12835992delinsCAT , CM000680.2:g.12835990_12835992delinsCAT	GRCh38
NC_000018.9:g.12835989_12835991delinsCAT , CM000680.1:g.12835989_12835991delinsCAT	GRCh37
NC_000018.8:g.12825989_12825991delinsCAT	NCBI36
NG_029116.1:g.53344_53346delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000309660.10:c.261+799_261+801delinsATG MANE Select	ENSP00000311857.3:n.261+799_261+801delins...
ENST00000645191.1:c.-37+799_-37+801delinsATG	ENSP00000493693.1:n.-37+799_-37+801delins...
ENST00000645816.1:c.261+799_261+801delinsATG	ENSP00000494336.1:n.261+799_261+801delins...
ENST00000646492.1:c.-37+799_-37+801delinsATG	ENSP00000496181.1:n.-37+799_-37+801delins...
ENST00000309660.9:c.261+799_261+801delinsATG	ENSP00000311857.3:n.261+799_261+801delins...
ENST00000327283.7:c.261+799_261+801delinsATG	ENSP00000320298.3:n.261+799_261+801delins...
ENST00000353319.8:c.261+799_261+801delinsATG	ENSP00000320546.3:n.261+799_261+801delins...
ENST00000587703.5:c.34+799_34+801delinsATG
ENST00000589216.1:c.*41+799_*41+801delinsATG	ENSP00000468408.1:n.*41+799_*41+801delins...
ENST00000591115.5:c.261+799_261+801delinsATG	ENSP00000466936.1:n.261+799_261+801delins...
ENST00000591305.5:c.*41+799_*41+801delinsATG	ENSP00000468012.1:n.*41+799_*41+801delins...
ENST00000591497.5:c.174+799_174+801delinsATG	ENSP00000467823.1:n.174+799_174+801delins...
ENST00000592059.5:c.-37+799_-37+801delinsATG	ENSP00000466206.1:n.-37+799_-37+801delins...
ENST00000592776.1:c.261+799_261+801delinsATG	ENSP00000468155.1:n.261+799_261+801delins...
NM_001207013.1:c.261+799_261+801delinsATG	NP_001193942.1:n.261+799_261+801delinsATG...
NM_001308287.1:c.174+799_174+801delinsATG	NP_001295216.1:n.174+799_174+801delinsATG...
NM_002828.3:c.261+799_261+801delinsATG	NP_002819.2:n.261+799_261+801delinsATG
NM_080422.2:c.261+799_261+801delinsATG	NP_536347.1:n.261+799_261+801delinsATG
NM_080423.2:c.261+799_261+801delinsATG	NP_536348.1:n.261+799_261+801delinsATG
XM_005258124.2:c.261+799_261+801delinsATG	XP_005258181.1:n.261+799_261+801delinsATG...
XM_005258125.2:c.261+799_261+801delinsATG	XP_005258182.1:n.261+799_261+801delinsATG...
XM_011525705.1:c.174+799_174+801delinsATG	XP_011524007.1:n.174+799_174+801delinsATG...
XM_011525706.1:c.261+799_261+801delinsATG	XP_011524008.1:n.261+799_261+801delinsATG...
XM_005258124.4:c.261+799_261+801delinsATG	XP_005258181.1:n.261+799_261+801delinsATG...
XM_005258125.4:c.261+799_261+801delinsATG	XP_005258182.1:n.261+799_261+801delinsATG...
XM_011525705.3:c.174+799_174+801delinsATG	XP_011524007.1:n.174+799_174+801delinsATG...
XM_011525706.2:c.261+799_261+801delinsATG	XP_011524008.1:n.261+799_261+801delinsATG...
XM_017025884.1:c.261+799_261+801delinsATG	XP_016881373.1:n.261+799_261+801delinsATG...
XM_017025885.2:c.174+799_174+801delinsATG	XP_016881374.1:n.174+799_174+801delinsATG...
XM_017025886.1:c.-37+799_-37+801delinsATG	XP_016881375.1:n.-37+799_-37+801delinsATG...
XM_017025887.2:c.-37+799_-37+801delinsATG	XP_016881376.1:n.-37+799_-37+801delinsATG...
XM_017025888.2:c.-37+799_-37+801delinsATG	XP_016881377.1:n.-37+799_-37+801delinsATG...
XM_024451228.1:c.261+799_261+801delinsATG	XP_024306996.1:n.261+799_261+801delinsATG...
XM_024451229.1:c.-37+799_-37+801delinsATG	XP_024306997.1:n.-37+799_-37+801delinsATG...
XM_024451230.1:c.-37+799_-37+801delinsATG	XP_024306998.1:n.-37+799_-37+801delinsATG...
NM_002828.4:c.261+799_261+801delinsATG MANE Select	NP_002819.2:n.261+799_261+801delinsATG
NM_001207013.2:c.261+799_261+801delinsATG	NP_001193942.1:n.261+799_261+801delinsATG...
NM_080422.3:c.261+799_261+801delinsATG	NP_536347.1:n.261+799_261+801delinsATG
NM_080423.3:c.261+799_261+801delinsATG	NP_536348.1:n.261+799_261+801delinsATG