Canonical Allele Identifier: CA674355894

Gene: PTPN5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18771813T>A , CM000673.2:g.18771813T>A	GRCh38
NC_000011.9:g.18793360T>A , CM000673.1:g.18793360T>A	GRCh37
NC_000011.8:g.18749936T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358540.7:c.20+126A>T MANE Select	ENSP00000351342.2:n.20+126A>T
ENST00000358540.6:c.20+126A>T	ENSP00000351342.2:n.20+126A>T
ENST00000396168.1:c.-52-5930A>T	ENSP00000379471.1:n.-52-5930A>T
ENST00000396170.5:c.20+126A>T	ENSP00000379473.1:n.20+126A>T
NM_001039970.1:c.20+126A>T	NP_001035059.1:n.20+126A>T
NM_001278236.1:c.20+126A>T	NP_001265165.1:n.20+126A>T
NM_001278238.1:c.-52-5930A>T	NP_001265167.1:n.-52-5930A>T
NM_001278239.1:c.-52-5930A>T	NP_001265168.1:n.-52-5930A>T
NM_006906.1:c.20+126A>T	NP_008837.1:n.20+126A>T
NM_032781.3:c.20+126A>T	NP_116170.3:n.20+126A>T
XM_011520411.1:c.20+126A>T	XP_011518713.1:n.20+126A>T
XM_011520411.3:c.20+126A>T	XP_011518713.1:n.20+126A>T
XM_017018434.2:c.20+126A>T	XP_016873923.1:n.20+126A>T
XM_017018435.2:c.20+126A>T	XP_016873924.1:n.20+126A>T
XM_017018436.1:c.-52-5930A>T	XP_016873925.1:n.-52-5930A>T
XM_017018437.1:c.20+126A>T	XP_016873926.1:n.20+126A>T
XM_017018439.1:c.-52-5930A>T	XP_016873928.1:n.-52-5930A>T
XM_017018440.2:c.20+126A>T	XP_016873929.1:n.20+126A>T
XM_017018441.2:c.20+126A>T	XP_016873930.1:n.20+126A>T
NM_006906.2:c.20+126A>T MANE Select	NP_008837.1:n.20+126A>T
NM_001039970.2:c.20+126A>T	NP_001035059.1:n.20+126A>T
NM_001278238.2:c.-52-5930A>T	NP_001265167.1:n.-52-5930A>T
NM_001278239.2:c.-52-5930A>T	NP_001265168.1:n.-52-5930A>T
NM_032781.4:c.20+126A>T	NP_116170.3:n.20+126A>T