Canonical Allele Identifier: CA2285454042

Gene: PTPN2

Linked Data

• dbSNP Id: rs2044514431

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12877055_12877064del , CM000680.2:g.12877055_12877064del	GRCh38
NC_000018.9:g.12877054_12877063del , CM000680.1:g.12877054_12877063del	GRCh37
NC_000018.8:g.12867054_12867063del	NCBI36
NG_029116.1:g.12275_12284del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309660.10:c.69+7012_69+7021del MANE Select	ENSP00000311857.3:n.69+7012_69+7021del
ENST00000643397.1:n.197+3435_197+3444del
ENST00000645191.1:c.-347-4792_-347-4783del	ENSP00000493693.1:n.-347-4792_-347-4783del
ENST00000645816.1:c.69+7012_69+7021del	ENSP00000494336.1:n.69+7012_69+7021del
ENST00000646492.1:c.-327+6557_-327+6566del	ENSP00000496181.1:n.-327+6557_-327+6566del
ENST00000309660.9:c.69+7012_69+7021del	ENSP00000311857.3:n.69+7012_69+7021del
ENST00000327283.7:c.69+7012_69+7021del	ENSP00000320298.3:n.69+7012_69+7021del
ENST00000353319.8:c.69+7012_69+7021del	ENSP00000320546.3:n.69+7012_69+7021del
ENST00000589216.1:c.69+7012_69+7021del	ENSP00000468408.1:n.69+7012_69+7021del
ENST00000591115.5:c.69+7012_69+7021del	ENSP00000466936.1:n.69+7012_69+7021del
ENST00000591305.5:c.69+7012_69+7021del	ENSP00000468012.1:n.69+7012_69+7021del
ENST00000592059.5:c.-228-17807_-228-17798del	ENSP00000466206.1:n.-228-17807_-228-17798del
ENST00000592776.1:c.69+7012_69+7021del	ENSP00000468155.1:n.69+7012_69+7021del
NM_001207013.1:c.69+7012_69+7021del	NP_001193942.1:n.69+7012_69+7021del
NM_002828.3:c.69+7012_69+7021del	NP_002819.2:n.69+7012_69+7021del
NM_080422.2:c.69+7012_69+7021del	NP_536347.1:n.69+7012_69+7021del
NM_080423.2:c.69+7012_69+7021del	NP_536348.1:n.69+7012_69+7021del
XM_005258124.2:c.69+7012_69+7021del	XP_005258181.1:n.69+7012_69+7021del
XM_005258125.2:c.69+7012_69+7021del	XP_005258182.1:n.69+7012_69+7021del
XM_011525706.1:c.69+7012_69+7021del	XP_011524008.1:n.69+7012_69+7021del
XM_005258124.4:c.69+7012_69+7021del	XP_005258181.1:n.69+7012_69+7021del
XM_005258125.4:c.69+7012_69+7021del	XP_005258182.1:n.69+7012_69+7021del
XM_011525706.2:c.69+7012_69+7021del	XP_011524008.1:n.69+7012_69+7021del
XM_017025884.1:c.69+7012_69+7021del	XP_016881373.1:n.69+7012_69+7021del
XM_017025886.1:c.-138+7012_-138+7021del	XP_016881375.1:n.-138+7012_-138+7021del
XM_017025887.2:c.-138+7012_-138+7021del	XP_016881376.1:n.-138+7012_-138+7021del
XM_017025888.2:c.-138+7012_-138+7021del	XP_016881377.1:n.-138+7012_-138+7021del
XM_024451228.1:c.69+7012_69+7021del	XP_024306996.1:n.69+7012_69+7021del
NM_002828.4:c.69+7012_69+7021del MANE Select	NP_002819.2:n.69+7012_69+7021del
NM_001207013.2:c.69+7012_69+7021del	NP_001193942.1:n.69+7012_69+7021del
NM_080422.3:c.69+7012_69+7021del	NP_536347.1:n.69+7012_69+7021del
NM_080423.3:c.69+7012_69+7021del	NP_536348.1:n.69+7012_69+7021del