Canonical Allele Identifier: CA2734641203
Gene: PTPN2 HGNC NCBI

Linked Data

dbSNP Id: rs2145334999

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12821511_12821512del , CM000680.2:g.12821511_12821512del GRCh38
NC_000018.9:g.12821510_12821511del , CM000680.1:g.12821510_12821511del GRCh37
NC_000018.8:g.12811510_12811511del NCBI36
NG_029116.1:g.67828_67829del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309660.10:c.496-4143_496-4142del MANE Select ENSP00000311857.3:n.496-4143_496-4142del
ENST00000645191.1:c.199-4143_199-4142del ENSP00000493693.1:n.199-4143_199-4142del
ENST00000645816.1:c.496-83_496-82del ENSP00000494336.1:n.496-83_496-82del
ENST00000646492.1:c.199-4143_199-4142del ENSP00000496181.1:n.199-4143_199-4142del
ENST00000309660.9:c.496-4143_496-4142del ENSP00000311857.3:n.496-4143_496-4142del
ENST00000327283.7:c.496-4143_496-4142del ENSP00000320298.3:n.496-4143_496-4142del
ENST00000353319.8:c.496-4143_496-4142del ENSP00000320546.3:n.496-4143_496-4142del
ENST00000587703.5:c.133+9435_133+9436del
ENST00000589216.1:c.*276-4143_*276-4142del ENSP00000468408.1:n.*276-4143_*276-4142del
ENST00000591115.5:c.496-2226_496-2225del ENSP00000466936.1:n.496-2226_496-2225del
ENST00000591305.5:c.*141-4143_*141-4142del ENSP00000468012.1:n.*141-4143_*141-4142del
ENST00000591497.5:c.409-4143_409-4142del ENSP00000467823.1:n.409-4143_409-4142del
ENST00000592776.1:c.496-4243_496-4242del ENSP00000468155.1:n.496-4243_496-4242del
NM_001207013.1:c.496-2226_496-2225del NP_001193942.1:n.496-2226_496-2225del
NM_001308287.1:c.409-4143_409-4142del NP_001295216.1:n.409-4143_409-4142del
NM_002828.3:c.496-4143_496-4142del NP_002819.2:n.496-4143_496-4142del
NM_080422.2:c.496-4143_496-4142del NP_536347.1:n.496-4143_496-4142del
NM_080423.2:c.496-4143_496-4142del NP_536348.1:n.496-4143_496-4142del
XM_005258124.2:c.496-2226_496-2225del XP_005258181.1:n.496-2226_496-2225del
XM_005258125.2:c.496-2226_496-2225del XP_005258182.1:n.496-2226_496-2225del
XM_011525705.1:c.409-2226_409-2225del XP_011524007.1:n.409-2226_409-2225del
XM_011525706.1:c.361-4143_361-4142del XP_011524008.1:n.361-4143_361-4142del
XM_005258124.4:c.496-2226_496-2225del XP_005258181.1:n.496-2226_496-2225del
XM_005258125.4:c.496-2226_496-2225del XP_005258182.1:n.496-2226_496-2225del
XM_011525705.3:c.409-2226_409-2225del XP_011524007.1:n.409-2226_409-2225del
XM_011525706.2:c.361-4143_361-4142del XP_011524008.1:n.361-4143_361-4142del
XM_017025884.1:c.496-4143_496-4142del XP_016881373.1:n.496-4143_496-4142del
XM_017025885.2:c.409-4143_409-4142del XP_016881374.1:n.409-4143_409-4142del
XM_017025886.1:c.199-4143_199-4142del XP_016881375.1:n.199-4143_199-4142del
XM_017025887.2:c.199-4143_199-4142del XP_016881376.1:n.199-4143_199-4142del
XM_017025888.2:c.199-4143_199-4142del XP_016881377.1:n.199-4143_199-4142del
XM_024451228.1:c.361-4143_361-4142del XP_024306996.1:n.361-4143_361-4142del
XM_024451229.1:c.199-4143_199-4142del XP_024306997.1:n.199-4143_199-4142del
XM_024451230.1:c.199-4143_199-4142del XP_024306998.1:n.199-4143_199-4142del
NM_002828.4:c.496-4143_496-4142del MANE Select NP_002819.2:n.496-4143_496-4142del
NM_001207013.2:c.496-2226_496-2225del NP_001193942.1:n.496-2226_496-2225del
NM_080422.3:c.496-4143_496-4142del NP_536347.1:n.496-4143_496-4142del
NM_080423.3:c.496-4143_496-4142del NP_536348.1:n.496-4143_496-4142del