Canonical Allele Identifier: CA13209136

Gene: PTPRE

Identifiers and link-outs to other resources

• dbSNP Id: rs10830196
• gnomAD: 10:129723712 C / T
• MyVariant Identifiers: chr10:g.129723712C>T (hg19) ; chr10:g.127925448C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.127925448C>T , CM000672.2:g.127925448C>T	GRCh38
NC_000010.10:g.129723712C>T , CM000672.1:g.129723712C>T	GRCh37
NC_000010.9:g.129613702C>T	NCBI36
NG_029511.1:g.23388C>T

Transcript Alleles

HGVS	Amino-acid change
NM_001316676.1:c.-169+18139C>T VV	NP_001303605.1:p.=
NM_006504.4:c.-31+18139C>T VV
NM_006504.5:c.-31+18139C>T VV	NP_006495.1:p.=
XM_011539993.1:c.53+18139C>T	XP_011538295.1:p.=
XM_011539994.1:c.53+18139C>T	XP_011538296.1:p.=
XM_011539995.1:c.53+18139C>T	XP_011538297.1:p.=
XM_011539996.1:c.53+18139C>T	XP_011538298.1:p.=
XM_011539998.1:c.53+18139C>T	XP_011538300.1:p.=
XR_945793.1:n.234+18139C>T
NM_001323355.1:c.53+18139C>T VV	NP_001310284.1:p.=
NM_001323356.1:c.53+18139C>T VV	NP_001310285.1:p.=
XM_011539994.2:c.53+18139C>T
XM_017016467.1:c.53+18139C>T	XP_016871956.1:p.=
XM_017016468.2:c.-31+18139C>T	XP_016871957.1:p.=
XM_017016469.2:c.53+18139C>T	XP_016871958.1:p.=
XM_024448092.1:c.-93-5530C>T	XP_024303860.1:p.=
XR_002956995.1:n.234+18139C>T
ENST00000254667.7:c.-31+18139C>T	ENSP00000254667.3:p.=
ENST00000442830.5:c.-202+18139C>T	ENSP00000410540.1:p.=