Canonical Allele Identifier: CA2785655487

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402927dup , CM000671.2:g.114402927dup	GRCh38
NC_000009.11:g.117165207dup , CM000671.1:g.117165207dup	GRCh37
NC_000009.10:g.116205028dup	NCBI36
NG_016700.1:g.107530dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.895dup	ENSP00000514396.1:p.Ser299PhefsTer?
ENST00000362057.4:c.2551dup MANE Select	ENSP00000354623.3:p.Ser851PhefsTer?
ENST00000674036.8:c.1524dup
ENST00000674048.1:n.2432dup
ENST00000265134.10:c.1402dup	ENSP00000265134.6:p.Ser468PhefsTer?
ENST00000362057.3:c.2551dup	ENSP00000354623.3:p.Ser851PhefsTer?
ENST00000374059.7:c.1498dup	ENSP00000363172.3:p.Ser500PhefsTer?
NM_001083885.2:c.1402dup	NP_001077354.2:p.Ser468PhefsTer?
NM_001173425.1:c.2548dup	NP_001166896.1:p.Ser850PhefsTer?
NM_015404.3:c.2551dup	NP_056219.3:p.Ser851PhefsTer?
XM_005251897.3:c.1888dup	XP_005251954.2:p.Ser630PhefsTer?
XM_011518484.1:c.2584dup	XP_011516786.1:p.Ser862PhefsTer?
XM_011518485.1:c.2584dup	XP_011516787.1:p.Ser862PhefsTer?
XM_011518486.1:c.2581dup	XP_011516788.1:p.Ser861PhefsTer?
XM_011518487.1:c.2458dup	XP_011516789.1:p.Ser820PhefsTer?
XM_011518488.1:c.2341dup	XP_011516790.1:p.Ser781PhefsTer?
XM_011518495.1:c.1261dup	XP_011516797.1:p.Ser421PhefsTer?
XR_929747.1:n.3488dup
XR_929748.1:n.3386dup
NM_001346890.1:c.1498dup	NP_001333819.1:p.Ser500PhefsTer?
XM_011518486.2:c.2581dup	XP_011516788.1:p.Ser861PhefsTer?
XM_011518487.2:c.2458dup	XP_011516789.1:p.Ser820PhefsTer?
XM_011518488.2:c.2341dup	XP_011516790.1:p.Ser781PhefsTer?
XR_929747.2:n.2799dup
XR_929748.2:n.2697dup
NM_015404.4:c.2551dup MANE Select	NP_056219.3:p.Ser851PhefsTer?
NM_001173425.2:c.2548dup	NP_001166896.1:p.Ser850PhefsTer?
NM_001083885.3:c.1402dup	NP_001077354.2:p.Ser468PhefsTer?