Canonical Allele Identifier: CA1873827848
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114407972A= , CM000671.2:g.114407972A= GRCh38
NC_000009.11:g.117170252A= , CM000671.1:g.117170252A= GRCh37
NC_000009.10:g.116210073A= NCBI36
NG_016700.1:g.102485T=

Transcript Alleles

HGVS Amino-acid change
ENST00000362057.4:c.1673T= MANE Select ENSP00000354623.3:p.Ile558=
ENST00000673811.1:n.2397T=
ENST00000674036.8:c.646T=
ENST00000674048.1:n.1554T=
ENST00000265134.10:c.524T= ENSP00000265134.6:p.Ile175=
ENST00000362057.3:c.1673T= ENSP00000354623.3:p.Ile558=
ENST00000374059.7:c.620T= ENSP00000363172.3:p.Ile207=
NM_001083885.2:c.524T= NP_001077354.2:p.Ile175=
NM_001173425.1:c.1673T= NP_001166896.1:p.Ile558=
NM_015404.3:c.1673T= NP_056219.3:p.Ile558=
XM_005251897.3:c.1010T= XP_005251954.2:p.Ile337=
XM_011518484.1:c.1706T= XP_011516786.1:p.Ile569=
XM_011518485.1:c.1706T= XP_011516787.1:p.Ile569=
XM_011518486.1:c.1706T= XP_011516788.1:p.Ile569=
XM_011518487.1:c.1580T= XP_011516789.1:p.Ile527=
XM_011518488.1:c.1463T= XP_011516790.1:p.Ile488=
XM_011518492.1:c.*58T= XP_011516794.1:n.*58T=
XM_011518495.1:c.383T= XP_011516797.1:p.Ile128=
XR_929747.1:n.2610T=
XR_929748.1:n.2508T=
XR_929750.1:n.2609T=
XR_929751.1:n.2516T=
XR_929757.1:n.2483T=
NM_001346890.1:c.620T= NP_001333819.1:p.Ile207=
XM_011518486.2:c.1706T= XP_011516788.1:p.Ile569=
XM_011518487.2:c.1580T= XP_011516789.1:p.Ile527=
XM_011518488.2:c.1463T= XP_011516790.1:p.Ile488=
XM_011518492.2:c.*58T= XP_011516794.1:n.*58T=
XR_929747.2:n.1921T=
XR_929748.2:n.1819T=
XR_929750.3:n.1920T=
XR_929757.2:n.1794T=
NM_015404.4:c.1673T= MANE Select NP_056219.3:p.Ile558=
NM_001173425.2:c.1673T= NP_001166896.1:p.Ile558=
NM_001083885.3:c.524T= NP_001077354.2:p.Ile175=