Canonical Allele Identifier: CA11407487
Gene: PTPRG HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10490775

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.62051050C>T , CM000665.2:g.62051050C>T GRCh38
NC_000003.11:g.62036724C>T , CM000665.1:g.62036724C>T GRCh37
NC_000003.10:g.62011764C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002841.3:c.520-27113C>T VV NP_002832.3:p.=
XM_005265352.3:c.478-27113C>T XP_005265409.1:p.=
XM_005265353.3:c.520-27113C>T XP_005265410.1:p.=
XM_017006961.2:c.640-27113C>T XP_016862450.1:p.=
XM_017006962.1:c.559-27113C>T XP_016862451.1:p.=
XM_017006963.2:c.640-27113C>T XP_016862452.1:p.=
XM_017006964.1:c.172-27113C>T XP_016862453.1:p.=
NM_002841.4:c.520-27113C>T VV MANE Preferred
ENST00000295874.14:c.520-27113C>T ENSP00000295874.10:p.=
ENST00000474889.5:c.520-27113C>T ENSP00000418112.1:p.=
ENST00000615556.3:n.334-27113C>T ENSP00000484346.1:p.=
ENST00000618938.2:n.334-27113C>T ENSP00000480407.1:p.=