Canonical Allele Identifier: CA2285426326

Gene: PTPN2

Linked Data

• dbSNP Id: rs2042271043

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12821632_12821640del , CM000680.2:g.12821632_12821640del	GRCh38
NC_000018.9:g.12821631_12821639del , CM000680.1:g.12821631_12821639del	GRCh37
NC_000018.8:g.12811631_12811639del	NCBI36
NG_029116.1:g.67696_67704del

Transcript Alleles

HGVS	Amino-acid change
ENST00000309660.10:c.495+4170_495+4178del MANE Select	ENSP00000311857.3:n.495+4170_495+4178del
ENST00000645191.1:c.198+4170_198+4178del	ENSP00000493693.1:n.198+4170_198+4178del
ENST00000645816.1:c.496-215_496-207del	ENSP00000494336.1:n.496-215_496-207del
ENST00000646492.1:c.198+4170_198+4178del	ENSP00000496181.1:n.198+4170_198+4178del
ENST00000309660.9:c.495+4170_495+4178del	ENSP00000311857.3:n.495+4170_495+4178del
ENST00000327283.7:c.495+4170_495+4178del	ENSP00000320298.3:n.495+4170_495+4178del
ENST00000353319.8:c.495+4170_495+4178del	ENSP00000320546.3:n.495+4170_495+4178del
ENST00000587703.5:c.133+9303_133+9311del
ENST00000589216.1:c.*275+4170_*275+4178del	ENSP00000468408.1:n.*275+4170_*275+4178del
ENST00000591115.5:c.496-2358_496-2350del	ENSP00000466936.1:n.496-2358_496-2350del
ENST00000591305.5:c.*141-4275_*141-4267del	ENSP00000468012.1:n.*141-4275_*141-4267del
ENST00000591497.5:c.408+4170_408+4178del	ENSP00000467823.1:n.408+4170_408+4178del
ENST00000592776.1:c.495+4170_495+4178del	ENSP00000468155.1:n.495+4170_495+4178del
NM_001207013.1:c.496-2358_496-2350del	NP_001193942.1:n.496-2358_496-2350del
NM_001308287.1:c.408+4170_408+4178del	NP_001295216.1:n.408+4170_408+4178del
NM_002828.3:c.495+4170_495+4178del	NP_002819.2:n.495+4170_495+4178del
NM_080422.2:c.495+4170_495+4178del	NP_536347.1:n.495+4170_495+4178del
NM_080423.2:c.495+4170_495+4178del	NP_536348.1:n.495+4170_495+4178del
XM_005258124.2:c.496-2358_496-2350del	XP_005258181.1:n.496-2358_496-2350del
XM_005258125.2:c.496-2358_496-2350del	XP_005258182.1:n.496-2358_496-2350del
XM_011525705.1:c.409-2358_409-2350del	XP_011524007.1:n.409-2358_409-2350del
XM_011525706.1:c.361-4275_361-4267del	XP_011524008.1:n.361-4275_361-4267del
XM_005258124.4:c.496-2358_496-2350del	XP_005258181.1:n.496-2358_496-2350del
XM_005258125.4:c.496-2358_496-2350del	XP_005258182.1:n.496-2358_496-2350del
XM_011525705.3:c.409-2358_409-2350del	XP_011524007.1:n.409-2358_409-2350del
XM_011525706.2:c.361-4275_361-4267del	XP_011524008.1:n.361-4275_361-4267del
XM_017025884.1:c.495+4170_495+4178del	XP_016881373.1:n.495+4170_495+4178del
XM_017025885.2:c.408+4170_408+4178del	XP_016881374.1:n.408+4170_408+4178del
XM_017025886.1:c.198+4170_198+4178del	XP_016881375.1:n.198+4170_198+4178del
XM_017025887.2:c.198+4170_198+4178del	XP_016881376.1:n.198+4170_198+4178del
XM_017025888.2:c.198+4170_198+4178del	XP_016881377.1:n.198+4170_198+4178del
XM_024451228.1:c.361-4275_361-4267del	XP_024306996.1:n.361-4275_361-4267del
XM_024451229.1:c.198+4170_198+4178del	XP_024306997.1:n.198+4170_198+4178del
XM_024451230.1:c.198+4170_198+4178del	XP_024306998.1:n.198+4170_198+4178del
NM_002828.4:c.495+4170_495+4178del MANE Select	NP_002819.2:n.495+4170_495+4178del
NM_001207013.2:c.496-2358_496-2350del	NP_001193942.1:n.496-2358_496-2350del
NM_080422.3:c.495+4170_495+4178del	NP_536347.1:n.495+4170_495+4178del
NM_080423.3:c.495+4170_495+4178del	NP_536348.1:n.495+4170_495+4178del