Canonical Allele Identifier: CA2838264160
Gene: PTPRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61562223dup , CM000665.2:g.61562223dup GRCh38
NC_000003.11:g.61547897dup , CM000665.1:g.61547897dup GRCh37
NC_000003.10:g.61522937dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474889.6:c.-65dup MANE Select ENSP00000418112.1:n.-65dup
ENST00000295874.14:c.-65dup ENSP00000295874.10:n.-65dup
ENST00000474889.5:c.-65dup ENSP00000418112.1:n.-65dup
ENST00000475527.1:n.373dup
ENST00000495879.1:n.655dup
NM_002841.3:c.-65dup NP_002832.3:n.-65dup
XM_005265353.3:c.-65dup XP_005265410.1:n.-65dup
XM_017006961.2:c.-65dup XP_016862450.1:n.-65dup
XM_017006963.2:c.-65dup XP_016862452.1:n.-65dup
NM_002841.4:c.-65dup MANE Select NP_002832.3:n.-65dup
NM_001375471.1:c.-65dup NP_001362400.1:n.-65dup