Canonical Allele Identifier: CA1873827850
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114407980C= , CM000671.2:g.114407980C= GRCh38
NC_000009.11:g.117170260C= , CM000671.1:g.117170260C= GRCh37
NC_000009.10:g.116210081C= NCBI36
NG_016700.1:g.102477G=

Transcript Alleles

HGVS Amino-acid change
ENST00000362057.4:c.1665G= MANE Select ENSP00000354623.3:p.Gln555=
ENST00000673811.1:n.2389G=
ENST00000674036.8:c.638G=
ENST00000674048.1:n.1546G=
ENST00000265134.10:c.516G= ENSP00000265134.6:p.Gln172=
ENST00000362057.3:c.1665G= ENSP00000354623.3:p.Gln555=
ENST00000374059.7:c.612G= ENSP00000363172.3:p.Gln204=
NM_001083885.2:c.516G= NP_001077354.2:p.Gln172=
NM_001173425.1:c.1665G= NP_001166896.1:p.Gln555=
NM_015404.3:c.1665G= NP_056219.3:p.Gln555=
XM_005251897.3:c.1002G= XP_005251954.2:p.Gln334=
XM_011518484.1:c.1698G= XP_011516786.1:p.Gln566=
XM_011518485.1:c.1698G= XP_011516787.1:p.Gln566=
XM_011518486.1:c.1698G= XP_011516788.1:p.Gln566=
XM_011518487.1:c.1572G= XP_011516789.1:p.Gln524=
XM_011518488.1:c.1455G= XP_011516790.1:p.Gln485=
XM_011518492.1:c.*50G= XP_011516794.1:n.*50G=
XM_011518495.1:c.375G= XP_011516797.1:p.Gln125=
XR_929747.1:n.2602G=
XR_929748.1:n.2500G=
XR_929750.1:n.2601G=
XR_929751.1:n.2508G=
XR_929757.1:n.2475G=
NM_001346890.1:c.612G= NP_001333819.1:p.Gln204=
XM_011518486.2:c.1698G= XP_011516788.1:p.Gln566=
XM_011518487.2:c.1572G= XP_011516789.1:p.Gln524=
XM_011518488.2:c.1455G= XP_011516790.1:p.Gln485=
XM_011518492.2:c.*50G= XP_011516794.1:n.*50G=
XR_929747.2:n.1913G=
XR_929748.2:n.1811G=
XR_929750.3:n.1912G=
XR_929757.2:n.1786G=
NM_015404.4:c.1665G= MANE Select NP_056219.3:p.Gln555=
NM_001173425.2:c.1665G= NP_001166896.1:p.Gln555=
NM_001083885.3:c.516G= NP_001077354.2:p.Gln172=