Canonical Allele Identifier: CA1873836079
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114426305C= , CM000671.2:g.114426305C= GRCh38
NC_000009.11:g.117188585C= , CM000671.1:g.117188585C= GRCh37
NC_000009.10:g.116228406C= NCBI36
NG_016700.1:g.84152G=

Transcript Alleles

HGVS Amino-acid change
ENST00000699486.1:c.796G= ENSP00000514397.1:p.Asp266=
ENST00000362057.4:c.1072G= MANE Select ENSP00000354623.3:p.Asp358=
ENST00000673811.1:n.820G=
ENST00000674036.8:c.255G=
ENST00000265134.10:c.-78G= ENSP00000265134.6:n.-78G=
ENST00000362057.3:c.1072G= ENSP00000354623.3:p.Asp358=
NM_001083885.2:c.-78G= NP_001077354.2:n.-78G=
NM_001173425.1:c.1072G= NP_001166896.1:p.Asp358=
NM_015404.3:c.1072G= NP_056219.3:p.Asp358=
XM_005251897.3:c.964-18287G= XP_005251954.2:n.964-18287G=
XM_011518484.1:c.1072G= XP_011516786.1:p.Asp358=
XM_011518485.1:c.1072G= XP_011516787.1:p.Asp358=
XM_011518486.1:c.1072G= XP_011516788.1:p.Asp358=
XM_011518487.1:c.946G= XP_011516789.1:p.Asp316=
XM_011518488.1:c.1072G= XP_011516790.1:p.Asp358=
XM_011518489.1:c.1072G= XP_011516791.1:p.Asp358=
XM_011518490.1:c.1072G= XP_011516792.1:p.Asp358=
XM_011518491.1:c.1072G= XP_011516793.1:p.Asp358=
XM_011518492.1:c.1072G= XP_011516794.1:p.Asp358=
XM_011518493.1:c.1072G= XP_011516795.1:p.Asp358=
XM_011518494.1:c.1072G= XP_011516796.1:p.Asp358=
XM_011518495.1:c.-157-1281G= XP_011516797.1:n.-157-1281G=
XR_929747.1:n.1780G=
XR_929748.1:n.1780G=
XR_929749.1:n.1780G=
XR_929750.1:n.1780G=
XR_929751.1:n.1780G=
XR_929752.1:n.1780G=
XR_929753.1:n.1780G=
XR_929754.1:n.1780G=
XR_929755.1:n.1780G=
XR_929756.1:n.1780G=
XR_929757.1:n.1780G=
XM_011518486.2:c.1072G= XP_011516788.1:p.Asp358=
XM_011518487.2:c.946G= XP_011516789.1:p.Asp316=
XM_011518488.2:c.1072G= XP_011516790.1:p.Asp358=
XM_011518489.3:c.1072G= XP_011516791.1:p.Asp358=
XM_011518491.3:c.1072G= XP_011516793.1:p.Asp358=
XM_011518492.2:c.1072G= XP_011516794.1:p.Asp358=
XM_011518494.3:c.1072G= XP_011516796.1:p.Asp358=
XR_929747.2:n.1091G=
XR_929748.2:n.1091G=
XR_929749.2:n.1091G=
XR_929750.3:n.1091G=
XR_929752.2:n.1091G=
XR_929753.3:n.1091G=
XR_929754.2:n.1091G=
XR_929755.3:n.1091G=
XR_929756.2:n.1091G=
XR_929757.2:n.1091G=
NM_015404.4:c.1072G= MANE Select NP_056219.3:p.Asp358=
NM_001173425.2:c.1072G= NP_001166896.1:p.Asp358=
NM_001083885.3:c.-78G= NP_001077354.2:n.-78G=