Canonical Allele Identifier: CA2736434945

Gene: PTPRT

Linked Data

• dbSNP Id: rs1060499749

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.42352288G>C , CM000682.2:g.42352288G>C	GRCh38
NC_000020.10:g.40980928G>C , CM000682.1:g.40980928G>C	GRCh37
NC_000020.9:g.40414342G>C	NCBI36
NG_033880.1:g.842630C>G
NG_033880.2:g.842630C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373187.6:c.1561-3C>G MANE Select	ENSP00000362283.1:n.1561-3C>G
ENST00000356100.6:c.1561-3C>G	ENSP00000348408.2:n.1561-3C>G
ENST00000373184.5:c.1561-3C>G	ENSP00000362280.1:n.1561-3C>G
ENST00000373187.5:c.1561-3C>G	ENSP00000362283.1:n.1561-3C>G
ENST00000373190.5:c.1561-3C>G	ENSP00000362286.1:n.1561-3C>G
ENST00000373193.7:c.1561-3C>G	ENSP00000362289.4:n.1561-3C>G
ENST00000373198.8:c.1561-3C>G	ENSP00000362294.4:n.1561-3C>G
ENST00000373201.5:c.1561-3C>G	ENSP00000362297.1:n.1561-3C>G
ENST00000612229.4:c.415-3C>G	ENSP00000481466.1:n.415-3C>G
ENST00000617474.1:c.*1419-3C>G	ENSP00000484248.1:n.*1419-3C>G
ENST00000618610.1:c.408-3C>G
NM_007050.5:c.1561-3C>G	NP_008981.4:n.1561-3C>G
NM_133170.3:c.1561-3C>G	NP_573400.3:n.1561-3C>G
XM_011528511.1:c.1561-3C>G	XP_011526813.1:n.1561-3C>G
XM_011528512.1:c.1561-3C>G	XP_011526814.1:n.1561-3C>G
XM_011528513.1:c.1561-3C>G	XP_011526815.1:n.1561-3C>G
XM_011528514.1:c.1561-3C>G	XP_011526816.1:n.1561-3C>G
XM_011528515.1:c.1561-3C>G	XP_011526817.1:n.1561-3C>G
XM_011528516.1:c.1561-3C>G	XP_011526818.1:n.1561-3C>G
XM_017027611.1:c.1576-3C>G	XP_016883100.1:n.1576-3C>G
XM_017027612.1:c.1576-3C>G	XP_016883101.1:n.1576-3C>G
XM_017027613.1:c.1576-3C>G	XP_016883102.1:n.1576-3C>G
XM_024451820.1:c.1561-3C>G	XP_024307588.1:n.1561-3C>G
NM_007050.6:c.1561-3C>G MANE Select	NP_008981.4:n.1561-3C>G
NM_133170.4:c.1561-3C>G	NP_573400.3:n.1561-3C>G
NM_001394024.1:c.1561-3C>G	NP_001380953.1:n.1561-3C>G
NM_001394025.1:c.1561-3C>G	NP_001380954.1:n.1561-3C>G
NM_001394026.1:c.1561-3C>G	NP_001380955.1:n.1561-3C>G