Canonical Allele Identifier: CA726495

Gene: PTPRU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.29282705G>A , CM000663.2:g.29282705G>A	GRCh38
NC_000001.10:g.29609217G>A , CM000663.1:g.29609217G>A	GRCh37
NC_000001.9:g.29481804G>A	NCBI36
NG_033965.1:g.51190G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_133178.4:c.1898G>A MANE Select	NP_573439.2:p.Arg633Gln
ENST00000373779.8:c.1898G>A MANE Select	ENSP00000362884.3:p.Arg633Gln
NM_001195001.1:c.1898G>A	NP_001181930.1:p.Arg633Gln
NM_001195001.2:c.1898G>A	NP_001181930.1:p.Arg633Gln
NM_005704.4:c.1898G>A	NP_005695.3:p.Arg633Gln
NM_005704.5:c.1898G>A	NP_005695.3:p.Arg633Gln
NM_133177.3:c.1898G>A	NP_573438.3:p.Arg633Gln
NM_133177.4:c.1898G>A	NP_573438.3:p.Arg633Gln
NM_133178.3:c.1898G>A	NP_573439.2:p.Arg633Gln
ENST00000345512.7:c.1898G>A	ENSP00000334941.5:p.Arg633Gln
ENST00000373779.7:c.1898G>A	ENSP00000362884.3:p.Arg633Gln
ENST00000415600.6:n.240G>A
ENST00000428026.6:c.1898G>A	ENSP00000392332.2:p.Arg633Gln
ENST00000460170.2:c.1898G>A	ENSP00000432906.1:p.Arg633Gln
XM_006710269.2:c.1898G>A	XP_006710332.1:p.Arg633Gln
XM_006710270.2:c.1898G>A	XP_006710333.1:p.Arg633Gln
XM_006710272.2:c.1682G>A	XP_006710335.1:p.Arg561Gln
XM_006710273.2:c.1103G>A	XP_006710336.1:p.Arg368Gln
XM_016999992.1:c.1898G>A	XP_016855481.1:p.Arg633Gln
XM_016999993.1:c.1898G>A	XP_016855482.1:p.Arg633Gln
XM_016999994.1:c.1898G>A	XP_016855483.1:p.Arg633Gln
XM_016999995.1:c.1103G>A	XP_016855484.1:p.Arg368Gln