Canonical Allele Identifier: CA909059082

Gene: PTPRG

Linked Data

• dbSNP Id: rs1173586877
• gnomAD v3: 3-62079019-A-G
• gnomAD v4: 3-62079019-A-G
• MyVariant Identifiers: chr3:g.62064693A>G (hg19) ; chr3:g.62079019A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.62079019A>G , CM000665.2:g.62079019A>G	GRCh38
NC_000003.11:g.62064693A>G , CM000665.1:g.62064693A>G	GRCh37
NC_000003.10:g.62039733A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000474889.6:c.615+761A>G MANE Select	ENSP00000418112.1:n.615+761A>G
ENST00000295874.14:c.615+761A>G	ENSP00000295874.10:n.615+761A>G
ENST00000474889.5:c.615+761A>G	ENSP00000418112.1:n.615+761A>G
ENST00000615556.3:c.429+761A>G	ENSP00000484346.1:n.429+761A>G
ENST00000618938.2:c.429+761A>G	ENSP00000480407.1:n.429+761A>G
NM_002841.3:c.615+761A>G	NP_002832.3:n.615+761A>G
XM_005265352.3:c.573+761A>G	XP_005265409.1:n.573+761A>G
XM_005265353.3:c.615+761A>G	XP_005265410.1:n.615+761A>G
XM_017006961.2:c.735+761A>G	XP_016862450.1:n.735+761A>G
XM_017006962.1:c.654+761A>G	XP_016862451.1:n.654+761A>G
XM_017006963.2:c.735+761A>G	XP_016862452.1:n.735+761A>G
XM_017006964.1:c.267+761A>G	XP_016862453.1:n.267+761A>G
NM_002841.4:c.615+761A>G MANE Select	NP_002832.3:n.615+761A>G
NM_001375471.1:c.615+761A>G	NP_001362400.1:n.615+761A>G