Canonical Allele Identifier: CA466778257

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117186764T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114424484T>A , CM000671.2:g.114424484T>A	GRCh38
NC_000009.11:g.117186764T>A , CM000671.1:g.117186764T>A	GRCh37
NC_000009.10:g.116226585T>A	NCBI36
NG_016700.1:g.85973A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.990A>T	ENSP00000514397.1:p.Thr330=
ENST00000362057.4:c.1266A>T MANE Select	ENSP00000354623.3:p.Thr422=
ENST00000673811.1:n.2200A>T
ENST00000674036.8:c.449A>T
ENST00000674048.1:n.1147A>T
ENST00000265134.10:c.117A>T	ENSP00000265134.6:p.Thr39=
ENST00000362057.3:c.1266A>T	ENSP00000354623.3:p.Thr422=
ENST00000374059.7:c.213A>T	ENSP00000363172.3:p.Thr71=
NM_001083885.2:c.117A>T	NP_001077354.2:p.Thr39=
NM_001173425.1:c.1266A>T	NP_001166896.1:p.Thr422=
NM_015404.3:c.1266A>T	NP_056219.3:p.Thr422=
XM_005251897.3:c.964-16466A>T	XP_005251954.2:n.964-16466A>T
XM_011518484.1:c.1266A>T	XP_011516786.1:p.Thr422=
XM_011518485.1:c.1266A>T	XP_011516787.1:p.Thr422=
XM_011518486.1:c.1266A>T	XP_011516788.1:p.Thr422=
XM_011518487.1:c.1140A>T	XP_011516789.1:p.Thr380=
XM_011518488.1:c.1266A>T	XP_011516790.1:p.Thr422=
XM_011518489.1:c.1266A>T	XP_011516791.1:p.Thr422=
XM_011518490.1:c.1266A>T	XP_011516792.1:p.Thr422=
XM_011518491.1:c.1266A>T	XP_011516793.1:p.Thr422=
XM_011518492.1:c.1266A>T	XP_011516794.1:p.Thr422=
XM_011518493.1:c.1266A>T	XP_011516795.1:p.Thr422=
XM_011518494.1:c.1266A>T	XP_011516796.1:p.Thr422=
XM_011518495.1:c.-58A>T	XP_011516797.1:n.-58A>T
XR_929747.1:n.1974A>T
XR_929748.1:n.1974A>T
XR_929749.1:n.1974A>T
XR_929750.1:n.1974A>T
XR_929751.1:n.1974A>T
XR_929752.1:n.1974A>T
XR_929753.1:n.1974A>T
XR_929754.1:n.1974A>T
XR_929755.1:n.1974A>T
XR_929756.1:n.1974A>T
XR_929757.1:n.1974A>T
NM_001346890.1:c.213A>T	NP_001333819.1:p.Thr71=
XM_011518486.2:c.1266A>T	XP_011516788.1:p.Thr422=
XM_011518487.2:c.1140A>T	XP_011516789.1:p.Thr380=
XM_011518488.2:c.1266A>T	XP_011516790.1:p.Thr422=
XM_011518489.3:c.1266A>T	XP_011516791.1:p.Thr422=
XM_011518491.3:c.1266A>T	XP_011516793.1:p.Thr422=
XM_011518492.2:c.1266A>T	XP_011516794.1:p.Thr422=
XM_011518494.3:c.1266A>T	XP_011516796.1:p.Thr422=
XR_929747.2:n.1285A>T
XR_929748.2:n.1285A>T
XR_929749.2:n.1285A>T
XR_929750.3:n.1285A>T
XR_929752.2:n.1285A>T
XR_929753.3:n.1285A>T
XR_929754.2:n.1285A>T
XR_929755.3:n.1285A>T
XR_929756.2:n.1285A>T
XR_929757.2:n.1285A>T
NM_015404.4:c.1266A>T MANE Select	NP_056219.3:p.Thr422=
NM_001173425.2:c.1266A>T	NP_001166896.1:p.Thr422=
NM_001083885.3:c.117A>T	NP_001077354.2:p.Thr39=