Canonical Allele Identifier: CA1873827854
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114407989C= , CM000671.2:g.114407989C= GRCh38
NC_000009.11:g.117170269C= , CM000671.1:g.117170269C= GRCh37
NC_000009.10:g.116210090C= NCBI36
NG_016700.1:g.102468G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362057.4:c.1656G= MANE Select ENSP00000354623.3:p.Glu552=
ENST00000673811.1:n.2380G=
ENST00000674036.8:c.629G=
ENST00000674048.1:n.1537G=
ENST00000265134.10:c.507G= ENSP00000265134.6:p.Glu169=
ENST00000362057.3:c.1656G= ENSP00000354623.3:p.Glu552=
ENST00000374059.7:c.603G= ENSP00000363172.3:p.Glu201=
NM_001083885.2:c.507G= NP_001077354.2:p.Glu169=
NM_001173425.1:c.1656G= NP_001166896.1:p.Glu552=
NM_015404.3:c.1656G= NP_056219.3:p.Glu552=
XM_005251897.3:c.993G= XP_005251954.2:p.Glu331=
XM_011518484.1:c.1689G= XP_011516786.1:p.Glu563=
XM_011518485.1:c.1689G= XP_011516787.1:p.Glu563=
XM_011518486.1:c.1689G= XP_011516788.1:p.Glu563=
XM_011518487.1:c.1563G= XP_011516789.1:p.Glu521=
XM_011518488.1:c.1446G= XP_011516790.1:p.Glu482=
XM_011518492.1:c.*41G= XP_011516794.1:n.*41G=
XM_011518495.1:c.366G= XP_011516797.1:p.Glu122=
XR_929747.1:n.2593G=
XR_929748.1:n.2491G=
XR_929750.1:n.2592G=
XR_929751.1:n.2499G=
XR_929757.1:n.2466G=
NM_001346890.1:c.603G= NP_001333819.1:p.Glu201=
XM_011518486.2:c.1689G= XP_011516788.1:p.Glu563=
XM_011518487.2:c.1563G= XP_011516789.1:p.Glu521=
XM_011518488.2:c.1446G= XP_011516790.1:p.Glu482=
XM_011518492.2:c.*41G= XP_011516794.1:n.*41G=
XR_929747.2:n.1904G=
XR_929748.2:n.1802G=
XR_929750.3:n.1903G=
XR_929757.2:n.1777G=
NM_015404.4:c.1656G= MANE Select NP_056219.3:p.Glu552=
NM_001173425.2:c.1656G= NP_001166896.1:p.Glu552=
NM_001083885.3:c.507G= NP_001077354.2:p.Glu169=