Canonical Allele Identifier: CA1369519004

Gene: PTPRG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.62079044_62079046delinsGTC , CM000665.2:g.62079044_62079046delinsGTC	GRCh38
NC_000003.11:g.62064718_62064720delinsGTC , CM000665.1:g.62064718_62064720delinsGTC	GRCh37
NC_000003.10:g.62039758_62039760delinsGTC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000474889.6:c.615+786_615+788delinsGTC MANE Select	ENSP00000418112.1:n.615+786_615+788delins...
ENST00000295874.14:c.615+786_615+788delinsGTC	ENSP00000295874.10:n.615+786_615+788delin...
ENST00000474889.5:c.615+786_615+788delinsGTC	ENSP00000418112.1:n.615+786_615+788delins...
ENST00000615556.3:c.429+786_429+788delinsGTC	ENSP00000484346.1:n.429+786_429+788delins...
ENST00000618938.2:c.429+786_429+788delinsGTC	ENSP00000480407.1:n.429+786_429+788delins...
NM_002841.3:c.615+786_615+788delinsGTC	NP_002832.3:n.615+786_615+788delinsGTC
XM_005265352.3:c.573+786_573+788delinsGTC	XP_005265409.1:n.573+786_573+788delinsGTC...
XM_005265353.3:c.615+786_615+788delinsGTC	XP_005265410.1:n.615+786_615+788delinsGTC...
XM_017006961.2:c.735+786_735+788delinsGTC	XP_016862450.1:n.735+786_735+788delinsGTC...
XM_017006962.1:c.654+786_654+788delinsGTC	XP_016862451.1:n.654+786_654+788delinsGTC...
XM_017006963.2:c.735+786_735+788delinsGTC	XP_016862452.1:n.735+786_735+788delinsGTC...
XM_017006964.1:c.267+786_267+788delinsGTC	XP_016862453.1:n.267+786_267+788delinsGTC...
NM_002841.4:c.615+786_615+788delinsGTC MANE Select	NP_002832.3:n.615+786_615+788delinsGTC
NM_001375471.1:c.615+786_615+788delinsGTC	NP_001362400.1:n.615+786_615+788delinsGTC...