Canonical Allele Identifier: CA1955757100

Gene: PTPN5

Linked Data

• dbSNP Id: rs1851380174

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18780726del , CM000673.2:g.18780726del	GRCh38
NC_000011.9:g.18802273del , CM000673.1:g.18802273del	GRCh37
NC_000011.8:g.18758849del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358540.7:c.-113-8654del MANE Select	ENSP00000351342.2:n.-113-8654del
ENST00000358540.6:c.-113-8654del	ENSP00000351342.2:n.-113-8654del
ENST00000396168.1:c.-53+10800del	ENSP00000379471.1:n.-53+10800del
ENST00000396170.5:c.-68-8699del	ENSP00000379473.1:n.-68-8699del
NM_001039970.1:c.-113-8654del	NP_001035059.1:n.-113-8654del
NM_001278236.1:c.-68-8699del	NP_001265165.1:n.-68-8699del
NM_001278238.1:c.-53+10800del	NP_001265167.1:n.-53+10800del
NM_001278239.1:c.-53+10800del	NP_001265168.1:n.-53+10800del
NM_006906.1:c.-113-8654del	NP_008837.1:n.-113-8654del
NM_032781.3:c.-68-8699del	NP_116170.3:n.-68-8699del
XM_011520411.1:c.-113-8654del	XP_011518713.1:n.-113-8654del
XM_011520411.3:c.-113-8654del	XP_011518713.1:n.-113-8654del
XM_017018434.2:c.-113-8654del	XP_016873923.1:n.-113-8654del
XM_017018435.2:c.-68-8699del	XP_016873924.1:n.-68-8699del
XM_017018436.1:c.-53+10800del	XP_016873925.1:n.-53+10800del
XM_017018437.1:c.-113-8654del	XP_016873926.1:n.-113-8654del
XM_017018439.1:c.-53+10800del	XP_016873928.1:n.-53+10800del
XM_017018440.2:c.-113-8654del	XP_016873929.1:n.-113-8654del
XM_017018441.2:c.-113-8654del	XP_016873930.1:n.-113-8654del
NM_006906.2:c.-113-8654del MANE Select	NP_008837.1:n.-113-8654del
NM_001039970.2:c.-113-8654del	NP_001035059.1:n.-113-8654del
NM_001278238.2:c.-53+10800del	NP_001265167.1:n.-53+10800del
NM_001278239.2:c.-53+10800del	NP_001265168.1:n.-53+10800del
NM_032781.4:c.-68-8699del	NP_116170.3:n.-68-8699del