Canonical Allele Identifier: CA466911624

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117168780T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406500T>A , CM000671.2:g.114406500T>A	GRCh38
NC_000009.11:g.117168780T>A , CM000671.1:g.117168780T>A	GRCh37
NC_000009.10:g.116208601T>A	NCBI36
NG_016700.1:g.103957A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.435A>T	ENSP00000514396.1:p.Thr145=
ENST00000362057.4:c.2091A>T MANE Select	ENSP00000354623.3:p.Thr697=
ENST00000674036.8:c.1064A>T
ENST00000674048.1:n.1972A>T
ENST00000265134.10:c.942A>T	ENSP00000265134.6:p.Thr314=
ENST00000362057.3:c.2091A>T	ENSP00000354623.3:p.Thr697=
ENST00000374059.7:c.1038A>T	ENSP00000363172.3:p.Thr346=
NM_001083885.2:c.942A>T	NP_001077354.2:p.Thr314=
NM_001173425.1:c.2091A>T	NP_001166896.1:p.Thr697=
NM_015404.3:c.2091A>T	NP_056219.3:p.Thr697=
XM_005251897.3:c.1428A>T	XP_005251954.2:p.Thr476=
XM_011518484.1:c.2124A>T	XP_011516786.1:p.Thr708=
XM_011518485.1:c.2124A>T	XP_011516787.1:p.Thr708=
XM_011518486.1:c.2124A>T	XP_011516788.1:p.Thr708=
XM_011518487.1:c.1998A>T	XP_011516789.1:p.Thr666=
XM_011518488.1:c.1881A>T	XP_011516790.1:p.Thr627=
XM_011518495.1:c.801A>T	XP_011516797.1:p.Thr267=
XR_929747.1:n.3028A>T
XR_929748.1:n.2926A>T
NM_001346890.1:c.1038A>T	NP_001333819.1:p.Thr346=
XM_011518486.2:c.2124A>T	XP_011516788.1:p.Thr708=
XM_011518487.2:c.1998A>T	XP_011516789.1:p.Thr666=
XM_011518488.2:c.1881A>T	XP_011516790.1:p.Thr627=
XR_929747.2:n.2339A>T
XR_929748.2:n.2237A>T
NM_015404.4:c.2091A>T MANE Select	NP_056219.3:p.Thr697=
NM_001173425.2:c.2091A>T	NP_001166896.1:p.Thr697=
NM_001083885.3:c.942A>T	NP_001077354.2:p.Thr314=