Canonical Allele Identifier: CA2838195803

Gene: PTPRU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.29317153C>A , CM000663.2:g.29317153C>A	GRCh38
NC_000001.10:g.29643665C>A , CM000663.1:g.29643665C>A	GRCh37
NC_000001.9:g.29516252C>A	NCBI36
NG_033965.1:g.85638C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373779.8:c.3514-595C>A MANE Select	ENSP00000362884.3:n.3514-595C>A
ENST00000345512.7:c.3544-595C>A	ENSP00000334941.5:n.3544-595C>A
ENST00000373779.7:c.3514-595C>A	ENSP00000362884.3:n.3514-595C>A
ENST00000428026.6:c.3505-595C>A	ENSP00000392332.2:n.3505-595C>A
ENST00000460170.2:c.3532-595C>A	ENSP00000432906.1:n.3532-595C>A
NM_001195001.1:c.3505-595C>A	NP_001181930.1:n.3505-595C>A
NM_005704.4:c.3544-595C>A	NP_005695.3:n.3544-595C>A
NM_133177.3:c.3532-595C>A	NP_573438.3:n.3532-595C>A
NM_133178.3:c.3514-595C>A	NP_573439.2:n.3514-595C>A
XM_006710269.2:c.3532-595C>A	XP_006710332.1:n.3532-595C>A
XM_006710270.2:c.3523-595C>A	XP_006710333.1:n.3523-595C>A
XM_006710272.2:c.3316-595C>A	XP_006710335.1:n.3316-595C>A
XM_006710273.2:c.2737-595C>A	XP_006710336.1:n.2737-595C>A
XM_011540458.1:c.1201-595C>A	XP_011538760.1:n.1201-595C>A
XM_016999992.1:c.3562-595C>A	XP_016855481.1:n.3562-595C>A
XM_016999993.1:c.3553-595C>A	XP_016855482.1:n.3553-595C>A
XM_016999994.1:c.3535-595C>A	XP_016855483.1:n.3535-595C>A
XM_016999995.1:c.2767-595C>A	XP_016855484.1:n.2767-595C>A
NM_133178.4:c.3514-595C>A MANE Select	NP_573439.2:n.3514-595C>A
NM_001195001.2:c.3505-595C>A	NP_001181930.1:n.3505-595C>A
NM_005704.5:c.3544-595C>A	NP_005695.3:n.3544-595C>A
NM_133177.4:c.3532-595C>A	NP_573438.3:n.3532-595C>A