Canonical Allele Identifier: CA14757347

Gene: PTPRT

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.42781261T>G , CM000682.2:g.42781261T>G	GRCh38
NC_000020.10:g.41409901T>G , CM000682.1:g.41409901T>G	GRCh37
NC_000020.9:g.40843315T>G	NCBI36
NG_033880.1:g.413657A>C
NG_033880.2:g.413657A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373187.6:c.487-962A>C MANE Select	ENSP00000362283.1:n.487-962A>C
ENST00000356100.6:c.487-962A>C	ENSP00000348408.2:n.487-962A>C
ENST00000373184.5:c.487-962A>C	ENSP00000362280.1:n.487-962A>C
ENST00000373187.5:c.487-962A>C	ENSP00000362283.1:n.487-962A>C
ENST00000373190.5:c.487-962A>C	ENSP00000362286.1:n.487-962A>C
ENST00000373193.7:c.487-962A>C	ENSP00000362289.4:n.487-962A>C
ENST00000373198.8:c.487-962A>C	ENSP00000362294.4:n.487-962A>C
ENST00000373201.5:c.487-962A>C	ENSP00000362297.1:n.487-962A>C
ENST00000617474.1:c.*345-962A>C	ENSP00000484248.1:n.*345-962A>C
ENST00000620410.1:c.274-962A>C	ENSP00000480136.1:n.274-962A>C
NM_007050.5:c.487-962A>C	NP_008981.4:n.487-962A>C
NM_133170.3:c.487-962A>C	NP_573400.3:n.487-962A>C
XM_011528511.1:c.487-962A>C	XP_011526813.1:n.487-962A>C
XM_011528512.1:c.487-962A>C	XP_011526814.1:n.487-962A>C
XM_011528513.1:c.487-962A>C	XP_011526815.1:n.487-962A>C
XM_011528514.1:c.487-962A>C	XP_011526816.1:n.487-962A>C
XM_011528515.1:c.487-962A>C	XP_011526817.1:n.487-962A>C
XM_011528516.1:c.487-962A>C	XP_011526818.1:n.487-962A>C
XM_017027611.1:c.502-962A>C	XP_016883100.1:n.502-962A>C
XM_017027612.1:c.502-962A>C	XP_016883101.1:n.502-962A>C
XM_017027613.1:c.502-962A>C	XP_016883102.1:n.502-962A>C
XM_024451820.1:c.487-962A>C	XP_024307588.1:n.487-962A>C
NM_007050.6:c.487-962A>C MANE Select	NP_008981.4:n.487-962A>C
NM_133170.4:c.487-962A>C	NP_573400.3:n.487-962A>C
NM_001394024.1:c.487-962A>C	NP_001380953.1:n.487-962A>C
NM_001394025.1:c.487-962A>C	NP_001380954.1:n.487-962A>C
NM_001394026.1:c.487-962A>C	NP_001380955.1:n.487-962A>C