Canonical Allele Identifier: CA13438377
Gene: PTPN5 HGNC NCBI

Linked Data

dbSNP Id: rs2278732
gnomAD v2: 11-18764113-G-A
gnomAD v3: 11-18742566-G-A
gnomAD v4: 11-18742566-G-A
MyVariant Identifiers: chr11:g.18764113G>A (hg19) chr11:g.18742566G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18742566G>A , CM000673.2:g.18742566G>A GRCh38
NC_000011.9:g.18764113G>A , CM000673.1:g.18764113G>A GRCh37
NC_000011.8:g.18720689G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000358540.7:c.484-63C>T MANE Select ENSP00000351342.2:n.484-63C>T
ENST00000358540.6:c.484-63C>T ENSP00000351342.2:n.484-63C>T
ENST00000396168.1:c.412-63C>T ENSP00000379471.1:n.412-63C>T
ENST00000396170.5:c.388-63C>T ENSP00000379473.1:n.388-63C>T
ENST00000477854.5:c.-105-63C>T ENSP00000435056.1:n.-105-63C>T
ENST00000496201.2:n.531-63C>T
NM_001039970.1:c.388-63C>T NP_001035059.1:n.388-63C>T
NM_001278236.1:c.388-63C>T NP_001265165.1:n.388-63C>T
NM_001278238.1:c.412-63C>T NP_001265167.1:n.412-63C>T
NM_001278239.1:c.316-63C>T NP_001265168.1:n.316-63C>T
NM_006906.1:c.484-63C>T NP_008837.1:n.484-63C>T
NM_032781.3:c.484-63C>T NP_116170.3:n.484-63C>T
XM_011520411.1:c.484-63C>T XP_011518713.1:n.484-63C>T
XM_011520412.1:c.367-63C>T XP_011518714.1:n.367-63C>T
XM_011520411.3:c.484-63C>T XP_011518713.1:n.484-63C>T
XM_017018434.2:c.484-63C>T XP_016873923.1:n.484-63C>T
XM_017018435.2:c.484-63C>T XP_016873924.1:n.484-63C>T
XM_017018436.1:c.412-63C>T XP_016873925.1:n.412-63C>T
XM_017018437.1:c.388-63C>T XP_016873926.1:n.388-63C>T
XM_017018438.2:c.367-63C>T XP_016873927.1:n.367-63C>T
XM_017018439.1:c.316-63C>T XP_016873928.1:n.316-63C>T
XM_017018440.2:c.484-63C>T XP_016873929.1:n.484-63C>T
XM_017018441.2:c.484-63C>T XP_016873930.1:n.484-63C>T
NM_006906.2:c.484-63C>T MANE Select NP_008837.1:n.484-63C>T
NM_001039970.2:c.388-63C>T NP_001035059.1:n.388-63C>T
NM_001278238.2:c.412-63C>T NP_001265167.1:n.412-63C>T
NM_001278239.2:c.316-63C>T NP_001265168.1:n.316-63C>T
NM_032781.4:c.484-63C>T NP_116170.3:n.484-63C>T
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