Canonical Allele Identifier: CA466910916

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165160T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402880T>C , CM000671.2:g.114402880T>C	GRCh38
NC_000009.11:g.117165160T>C , CM000671.1:g.117165160T>C	GRCh37
NC_000009.10:g.116204981T>C	NCBI36
NG_016700.1:g.107577A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.942A>G	ENSP00000514396.1:p.Glu314=
ENST00000362057.4:c.2598A>G MANE Select	ENSP00000354623.3:p.Glu866=
ENST00000674036.8:c.1571A>G
ENST00000674048.1:n.2479A>G
ENST00000265134.10:c.1449A>G	ENSP00000265134.6:p.Glu483=
ENST00000362057.3:c.2598A>G	ENSP00000354623.3:p.Glu866=
ENST00000374059.7:c.1545A>G	ENSP00000363172.3:p.Glu515=
NM_001083885.2:c.1449A>G	NP_001077354.2:p.Glu483=
NM_001173425.1:c.2595A>G	NP_001166896.1:p.Glu865=
NM_015404.3:c.2598A>G	NP_056219.3:p.Glu866=
XM_005251897.3:c.1935A>G	XP_005251954.2:p.Glu645=
XM_011518484.1:c.2631A>G	XP_011516786.1:p.Glu877=
XM_011518485.1:c.2631A>G	XP_011516787.1:p.Glu877=
XM_011518486.1:c.2628A>G	XP_011516788.1:p.Glu876=
XM_011518487.1:c.2505A>G	XP_011516789.1:p.Glu835=
XM_011518488.1:c.2388A>G	XP_011516790.1:p.Glu796=
XM_011518495.1:c.1308A>G	XP_011516797.1:p.Glu436=
NM_001346890.1:c.1545A>G	NP_001333819.1:p.Glu515=
XM_011518486.2:c.2628A>G	XP_011516788.1:p.Glu876=
XM_011518487.2:c.2505A>G	XP_011516789.1:p.Glu835=
XM_011518488.2:c.2388A>G	XP_011516790.1:p.Glu796=
NM_015404.4:c.2598A>G MANE Select	NP_056219.3:p.Glu866=
NM_001173425.2:c.2595A>G	NP_001166896.1:p.Glu865=
NM_001083885.3:c.1449A>G	NP_001077354.2:p.Glu483=