Canonical Allele Identifier: CA2285454072

Gene: PTPN2

Linked Data

• dbSNP Id: rs2044516445

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12877110G>C , CM000680.2:g.12877110G>C	GRCh38
NC_000018.9:g.12877109G>C , CM000680.1:g.12877109G>C	GRCh37
NC_000018.8:g.12867109G>C	NCBI36
NG_029116.1:g.12226C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309660.10:c.69+6963C>G MANE Select	ENSP00000311857.3:n.69+6963C>G
ENST00000643397.1:n.197+3386C>G
ENST00000645191.1:c.-347-4841C>G	ENSP00000493693.1:n.-347-4841C>G
ENST00000645816.1:c.69+6963C>G	ENSP00000494336.1:n.69+6963C>G
ENST00000646492.1:c.-327+6508C>G	ENSP00000496181.1:n.-327+6508C>G
ENST00000309660.9:c.69+6963C>G	ENSP00000311857.3:n.69+6963C>G
ENST00000327283.7:c.69+6963C>G	ENSP00000320298.3:n.69+6963C>G
ENST00000353319.8:c.69+6963C>G	ENSP00000320546.3:n.69+6963C>G
ENST00000589216.1:c.69+6963C>G	ENSP00000468408.1:n.69+6963C>G
ENST00000591115.5:c.69+6963C>G	ENSP00000466936.1:n.69+6963C>G
ENST00000591305.5:c.69+6963C>G	ENSP00000468012.1:n.69+6963C>G
ENST00000592059.5:c.-228-17856C>G	ENSP00000466206.1:n.-228-17856C>G
ENST00000592776.1:c.69+6963C>G	ENSP00000468155.1:n.69+6963C>G
NM_001207013.1:c.69+6963C>G	NP_001193942.1:n.69+6963C>G
NM_002828.3:c.69+6963C>G	NP_002819.2:n.69+6963C>G
NM_080422.2:c.69+6963C>G	NP_536347.1:n.69+6963C>G
NM_080423.2:c.69+6963C>G	NP_536348.1:n.69+6963C>G
XM_005258124.2:c.69+6963C>G	XP_005258181.1:n.69+6963C>G
XM_005258125.2:c.69+6963C>G	XP_005258182.1:n.69+6963C>G
XM_011525706.1:c.69+6963C>G	XP_011524008.1:n.69+6963C>G
XM_005258124.4:c.69+6963C>G	XP_005258181.1:n.69+6963C>G
XM_005258125.4:c.69+6963C>G	XP_005258182.1:n.69+6963C>G
XM_011525706.2:c.69+6963C>G	XP_011524008.1:n.69+6963C>G
XM_017025884.1:c.69+6963C>G	XP_016881373.1:n.69+6963C>G
XM_017025886.1:c.-138+6963C>G	XP_016881375.1:n.-138+6963C>G
XM_017025887.2:c.-138+6963C>G	XP_016881376.1:n.-138+6963C>G
XM_017025888.2:c.-138+6963C>G	XP_016881377.1:n.-138+6963C>G
XM_024451228.1:c.69+6963C>G	XP_024306996.1:n.69+6963C>G
NM_002828.4:c.69+6963C>G MANE Select	NP_002819.2:n.69+6963C>G
NM_001207013.2:c.69+6963C>G	NP_001193942.1:n.69+6963C>G
NM_080422.3:c.69+6963C>G	NP_536347.1:n.69+6963C>G
NM_080423.3:c.69+6963C>G	NP_536348.1:n.69+6963C>G