Canonical Allele Identifier: CA2209437946

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14765051_14765052delinsTG , CM000678.2:g.14765051_14765052delinsTG GRCh38
NC_000016.9:g.14858908_14858909delinsTG , CM000678.1:g.14858908_14858909delinsTG GRCh37
NC_000016.8:g.14766409_14766410delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000529166.6:c.748_749delinsTG (NPIPA2) MANE Select ENSP00000432029.1:p.Trp250=
ENST00000529166.5:c.748_749delinsTG (NPIPA2) ENSP00000432029.1:p.Trp250=
ENST00000553201.1:c.691_692delinsTG (NPIPA2) ENSP00000446882.1:p.Trp231=
ENST00000618714.4:c.63+14176_63+14177delinsTG (NPIPA1) ENSP00000484994.1:n.63+14176_63+14177delinsTG
ENST00000619019.3:c.902-211_902-210delinsTG (NPIPA3) ENSP00000479725.1:n.902-211_902-210delinsTG
ENST00000621766.4:c.691_692delinsTG (NPIPA3) ENSP00000483111.1:p.Trp231=
NM_001277324.1:c.691_692delinsTG (NPIPA2) NP_001264253.1:p.Trp231=
XM_005255489.2:c.691_692delinsTG (NPIPA2) XP_005255546.1:p.Trp231=
XM_006720917.2:c.*62_*63delinsTG (NPIPA2) XP_006720980.2:n.*62_*63delinsTG
XR_933118.1:n.168+1350_168+1351delinsCA
XR_933119.1:n.168+1350_168+1351delinsCA
XR_933120.1:n.168+1350_168+1351delinsCA
XM_011522595.2:c.*194_*195delinsTG (NPIPA2) XP_011520897.1:n.*194_*195delinsTG
XM_024450381.1:c.835_836delinsTG (NPIPA2) XP_024306149.1:p.Trp279=
XM_024450382.1:c.835_836delinsTG (NPIPA2) XP_024306150.1:p.Trp279=
XM_024450383.1:c.835_836delinsTG (NPIPA2) XP_024306151.1:p.Trp279=
XM_024450384.1:c.772_773delinsTG (NPIPA2) XP_024306152.1:p.Trp258=
XM_024450385.1:c.748_749delinsTG (NPIPA2) XP_024306153.1:p.Trp250=
XM_024450386.1:c.748_749delinsTG (NPIPA2) XP_024306154.1:p.Trp250=
XM_024450387.1:c.835_836delinsTG (NPIPA2) XP_024306155.1:p.Trp279=
XM_024450388.1:c.703_704delinsTG (NPIPA2) XP_024306156.1:p.Trp235=
XR_933118.2:n.168+1350_168+1351delinsCA
XR_933120.2:n.168+1350_168+1351delinsCA
NM_001277324.3:c.691_692delinsTG (NPIPA2) NP_001264253.1:p.Trp231=
NM_001395485.2:c.748_749delinsTG (NPIPA2) MANE Select NP_001382414.1:p.Trp250=
NM_001395486.2:c.748_749delinsTG (NPIPA2) NP_001382415.1:p.Trp250=