Canonical Allele Identifier: CA1955757093

Gene: PTPN5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18780712C= , CM000673.2:g.18780712C=	GRCh38
NC_000011.9:g.18802259C= , CM000673.1:g.18802259C=	GRCh37
NC_000011.8:g.18758835C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358540.7:c.-113-8641G= MANE Select	ENSP00000351342.2:n.-113-8641G=
ENST00000358540.6:c.-113-8641G=	ENSP00000351342.2:n.-113-8641G=
ENST00000396168.1:c.-53+10813G=	ENSP00000379471.1:n.-53+10813G=
ENST00000396170.5:c.-68-8686G=	ENSP00000379473.1:n.-68-8686G=
NM_001039970.1:c.-113-8641G=	NP_001035059.1:n.-113-8641G=
NM_001278236.1:c.-68-8686G=	NP_001265165.1:n.-68-8686G=
NM_001278238.1:c.-53+10813G=	NP_001265167.1:n.-53+10813G=
NM_001278239.1:c.-53+10813G=	NP_001265168.1:n.-53+10813G=
NM_006906.1:c.-113-8641G=	NP_008837.1:n.-113-8641G=
NM_032781.3:c.-68-8686G=	NP_116170.3:n.-68-8686G=
XM_011520411.1:c.-113-8641G=	XP_011518713.1:n.-113-8641G=
XM_011520411.3:c.-113-8641G=	XP_011518713.1:n.-113-8641G=
XM_017018434.2:c.-113-8641G=	XP_016873923.1:n.-113-8641G=
XM_017018435.2:c.-68-8686G=	XP_016873924.1:n.-68-8686G=
XM_017018436.1:c.-53+10813G=	XP_016873925.1:n.-53+10813G=
XM_017018437.1:c.-113-8641G=	XP_016873926.1:n.-113-8641G=
XM_017018439.1:c.-53+10813G=	XP_016873928.1:n.-53+10813G=
XM_017018440.2:c.-113-8641G=	XP_016873929.1:n.-113-8641G=
XM_017018441.2:c.-113-8641G=	XP_016873930.1:n.-113-8641G=
NM_006906.2:c.-113-8641G= MANE Select	NP_008837.1:n.-113-8641G=
NM_001039970.2:c.-113-8641G=	NP_001035059.1:n.-113-8641G=
NM_001278238.2:c.-53+10813G=	NP_001265167.1:n.-53+10813G=
NM_001278239.2:c.-53+10813G=	NP_001265168.1:n.-53+10813G=
NM_032781.4:c.-68-8686G=	NP_116170.3:n.-68-8686G=