Canonical Allele Identifier: CA2833740114

Gene: PTPRG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.62079032T>C , CM000665.2:g.62079032T>C	GRCh38
NC_000003.11:g.62064706T>C , CM000665.1:g.62064706T>C	GRCh37
NC_000003.10:g.62039746T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474889.6:c.615+774T>C MANE Select	ENSP00000418112.1:n.615+774T>C
ENST00000295874.14:c.615+774T>C	ENSP00000295874.10:n.615+774T>C
ENST00000474889.5:c.615+774T>C	ENSP00000418112.1:n.615+774T>C
ENST00000615556.3:c.429+774T>C	ENSP00000484346.1:n.429+774T>C
ENST00000618938.2:c.429+774T>C	ENSP00000480407.1:n.429+774T>C
NM_002841.3:c.615+774T>C	NP_002832.3:n.615+774T>C
XM_005265352.3:c.573+774T>C	XP_005265409.1:n.573+774T>C
XM_005265353.3:c.615+774T>C	XP_005265410.1:n.615+774T>C
XM_017006961.2:c.735+774T>C	XP_016862450.1:n.735+774T>C
XM_017006962.1:c.654+774T>C	XP_016862451.1:n.654+774T>C
XM_017006963.2:c.735+774T>C	XP_016862452.1:n.735+774T>C
XM_017006964.1:c.267+774T>C	XP_016862453.1:n.267+774T>C
NM_002841.4:c.615+774T>C MANE Select	NP_002832.3:n.615+774T>C
NM_001375471.1:c.615+774T>C	NP_001362400.1:n.615+774T>C