Canonical Allele Identifier: CA2365061010

Gene: PTPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.42885815A= , CM000682.2:g.42885815A=	GRCh38
NC_000020.10:g.41514455A= , CM000682.1:g.41514455A=	GRCh37
NC_000020.9:g.40947869A=	NCBI36
NG_033880.1:g.309103T=
NG_033880.2:g.309103T=

Transcript Alleles

HGVS	Amino-acid Change
NM_007050.6:c.206T= MANE Select	NP_008981.4:p.Val69=
ENST00000373187.6:c.206T= MANE Select	ENSP00000362283.1:p.Val69=
NM_001394024.1:c.206T=	NP_001380953.1:p.Val69=
NM_001394025.1:c.206T=	NP_001380954.1:p.Val69=
NM_001394026.1:c.206T=	NP_001380955.1:p.Val69=
NM_007050.5:c.206T=	NP_008981.4:p.Val69=
NM_133170.3:c.206T=	NP_573400.3:p.Val69=
NM_133170.4:c.206T=	NP_573400.3:p.Val69=
ENST00000356100.6:c.206T=	ENSP00000348408.2:p.Val69=
ENST00000373184.5:c.206T=	ENSP00000362280.1:p.Val69=
ENST00000373187.5:c.206T=	ENSP00000362283.1:p.Val69=
ENST00000373190.5:c.206T=	ENSP00000362286.1:p.Val69=
ENST00000373193.7:c.206T=	ENSP00000362289.4:p.Val69=
ENST00000373198.8:c.206T=	ENSP00000362294.4:p.Val69=
ENST00000373201.5:c.206T=	ENSP00000362297.1:p.Val69=
ENST00000617474.1:c.*64T=	ENSP00000484248.1:n.*64T=
XM_011528511.1:c.206T=	XP_011526813.1:p.Val69=
XM_011528512.1:c.206T=	XP_011526814.1:p.Val69=
XM_011528513.1:c.206T=	XP_011526815.1:p.Val69=
XM_011528514.1:c.206T=	XP_011526816.1:p.Val69=
XM_011528515.1:c.206T=	XP_011526817.1:p.Val69=
XM_011528516.1:c.206T=	XP_011526818.1:p.Val69=
XM_017027611.1:c.221T=	XP_016883100.1:p.Val74=
XM_017027612.1:c.221T=	XP_016883101.1:p.Val74=
XM_017027613.1:c.221T=	XP_016883102.1:p.Val74=
XM_024451820.1:c.206T=	XP_024307588.1:p.Val69=