Canonical Allele Identifier: CA374618865

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165099C>T (hg19) ; chr9:g.114402819C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402819C>T , CM000671.2:g.114402819C>T	GRCh38
NC_000009.11:g.117165099C>T , CM000671.1:g.117165099C>T	GRCh37
NC_000009.10:g.116204920C>T	NCBI36
NG_016700.1:g.107638G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1003G>A	ENSP00000514396.1:p.Ala335Thr
ENST00000362057.4:c.2659G>A MANE Select	ENSP00000354623.3:p.Ala887Thr
ENST00000674036.8:c.1632G>A
ENST00000674048.1:n.2540G>A
ENST00000265134.10:c.1510G>A	ENSP00000265134.6:p.Ala504Thr
ENST00000362057.3:c.2659G>A	ENSP00000354623.3:p.Ala887Thr
ENST00000374059.7:c.1606G>A	ENSP00000363172.3:p.Ala536Thr
NM_001083885.2:c.1510G>A	NP_001077354.2:p.Ala504Thr
NM_001173425.1:c.2656G>A	NP_001166896.1:p.Ala886Thr
NM_015404.3:c.2659G>A	NP_056219.3:p.Ala887Thr
XM_005251897.3:c.1996G>A	XP_005251954.2:p.Ala666Thr
XM_011518484.1:c.2692G>A	XP_011516786.1:p.Ala898Thr
XM_011518485.1:c.2692G>A	XP_011516787.1:p.Ala898Thr
XM_011518486.1:c.2689G>A	XP_011516788.1:p.Ala897Thr
XM_011518487.1:c.2566G>A	XP_011516789.1:p.Ala856Thr
XM_011518488.1:c.2449G>A	XP_011516790.1:p.Ala817Thr
XM_011518495.1:c.1369G>A	XP_011516797.1:p.Ala457Thr
NM_001346890.1:c.1606G>A	NP_001333819.1:p.Ala536Thr
XM_011518486.2:c.2689G>A	XP_011516788.1:p.Ala897Thr
XM_011518487.2:c.2566G>A	XP_011516789.1:p.Ala856Thr
XM_011518488.2:c.2449G>A	XP_011516790.1:p.Ala817Thr
NM_015404.4:c.2659G>A MANE Select	NP_056219.3:p.Ala887Thr
NM_001173425.2:c.2656G>A	NP_001166896.1:p.Ala886Thr
NM_001083885.3:c.1510G>A	NP_001077354.2:p.Ala504Thr