Canonical Allele Identifier: CA1369519038
Gene: PTPRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.62079079_62079099delinsAAGGAAAGTTAAAGACATAAG , CM000665.2:g.62079079_62079099delinsAAGGAAAGTTAAAGACATAAG GRCh38
NC_000003.11:g.62064753_62064773delinsAAGGAAAGTTAAAGACATAAG , CM000665.1:g.62064753_62064773delinsAAGGAAAGTTAAAGACATAAG GRCh37
NC_000003.10:g.62039793_62039813delinsAAGGAAAGTTAAAGACATAAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474889.6:c.615+821_615+841delinsAAGGAAAGTTAAAGACATAAG MANE Select ENSP00000418112.1:n.615+821_615+841delins...
ENST00000295874.14:c.615+821_615+841delinsAAGGAAAGTTAAAGACATAAG ENSP00000295874.10:n.615+821_615+841delin...
ENST00000474889.5:c.615+821_615+841delinsAAGGAAAGTTAAAGACATAAG ENSP00000418112.1:n.615+821_615+841delins...
ENST00000615556.3:c.429+821_429+841delinsAAGGAAAGTTAAAGACATAAG ENSP00000484346.1:n.429+821_429+841delins...
ENST00000618938.2:c.429+821_429+841delinsAAGGAAAGTTAAAGACATAAG ENSP00000480407.1:n.429+821_429+841delins...
NM_002841.3:c.615+821_615+841delinsAAGGAAAGTTAAAGACATAAG NP_002832.3:n.615+821_615+841delinsAAGGAA...
XM_005265352.3:c.573+821_573+841delinsAAGGAAAGTTAAAGACATAAG XP_005265409.1:n.573+821_573+841delinsAAG...
XM_005265353.3:c.615+821_615+841delinsAAGGAAAGTTAAAGACATAAG XP_005265410.1:n.615+821_615+841delinsAAG...
XM_017006961.2:c.735+821_735+841delinsAAGGAAAGTTAAAGACATAAG XP_016862450.1:n.735+821_735+841delinsAAG...
XM_017006962.1:c.654+821_654+841delinsAAGGAAAGTTAAAGACATAAG XP_016862451.1:n.654+821_654+841delinsAAG...
XM_017006963.2:c.735+821_735+841delinsAAGGAAAGTTAAAGACATAAG XP_016862452.1:n.735+821_735+841delinsAAG...
XM_017006964.1:c.267+821_267+841delinsAAGGAAAGTTAAAGACATAAG XP_016862453.1:n.267+821_267+841delinsAAG...
NM_002841.4:c.615+821_615+841delinsAAGGAAAGTTAAAGACATAAG MANE Select NP_002832.3:n.615+821_615+841delinsAAGGAA...
NM_001375471.1:c.615+821_615+841delinsAAGGAAAGTTAAAGACATAAG NP_001362400.1:n.615+821_615+841delinsAAG...