Canonical Allele Identifier: CA744463547
Gene: PTPRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.42076024C>T , CM000682.2:g.42076024C>T GRCh38
NC_000020.10:g.40704664C>T , CM000682.1:g.40704664C>T GRCh37
NC_000020.9:g.40138078C>T NCBI36
NG_033880.1:g.1118894G>A
NG_033880.2:g.1118894G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373187.6:c.*4855G>A MANE Select ENSP00000362283.1:n.*4855G>A
ENST00000356100.6:c.9208G>A ENSP00000348408.2:n.9208G>A
ENST00000373184.5:c.9211G>A ENSP00000362280.1:n.9211G>A
ENST00000373187.5:c.9181G>A ENSP00000362283.1:n.9181G>A
ENST00000373190.5:c.*4855G>A ENSP00000362286.1:n.*4855G>A
ENST00000373193.7:c.*4855G>A ENSP00000362289.4:n.*4855G>A
ENST00000373198.8:c.*4855G>A ENSP00000362294.4:n.*4855G>A
ENST00000373201.5:c.*4855G>A ENSP00000362297.1:n.*4855G>A
ENST00000612229.4:c.8035G>A ENSP00000481466.1:n.8035G>A
NM_007050.5:c.*4855G>A NP_008981.4:n.*4855G>A
NM_133170.3:c.*4855G>A NP_573400.3:n.*4855G>A
XM_011528511.1:c.*4855G>A XP_011526813.1:n.*4855G>A
XM_011528512.1:c.*878G>A XP_011526814.1:n.*878G>A
XM_011528513.1:c.*4855G>A XP_011526815.1:n.*4855G>A
XM_011528514.1:c.*4855G>A XP_011526816.1:n.*4855G>A
XM_011528515.1:c.*4855G>A XP_011526817.1:n.*4855G>A
XM_017027611.1:c.*4855G>A XP_016883100.1:n.*4855G>A
XM_017027612.1:c.*4855G>A XP_016883101.1:n.*4855G>A
XM_017027613.1:c.*4855G>A XP_016883102.1:n.*4855G>A
XM_024451820.1:c.4512+5858G>A XP_024307588.1:n.4512+5858G>A
XR_001754609.1:n.381-14555C>T
XR_001754610.1:n.525-14555C>T
XR_001754611.1:n.386-14555C>T
NM_007050.6:c.*4855G>A MANE Select NP_008981.4:n.*4855G>A
NM_133170.4:c.*4855G>A NP_573400.3:n.*4855G>A
NM_001394024.1:c.*4855G>A NP_001380953.1:n.*4855G>A
NM_001394025.1:c.*4855G>A NP_001380954.1:n.*4855G>A
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