Canonical Allele Identifier: CA374618953

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165147T>A (hg19) ; chr9:g.114402867T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402867T>A , CM000671.2:g.114402867T>A	GRCh38
NC_000009.11:g.117165147T>A , CM000671.1:g.117165147T>A	GRCh37
NC_000009.10:g.116204968T>A	NCBI36
NG_016700.1:g.107590A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.955A>T	ENSP00000514396.1:p.Thr319Ser
ENST00000362057.4:c.2611A>T MANE Select	ENSP00000354623.3:p.Thr871Ser
ENST00000674036.8:c.1584A>T
ENST00000674048.1:n.2492A>T
ENST00000265134.10:c.1462A>T	ENSP00000265134.6:p.Thr488Ser
ENST00000362057.3:c.2611A>T	ENSP00000354623.3:p.Thr871Ser
ENST00000374059.7:c.1558A>T	ENSP00000363172.3:p.Thr520Ser
NM_001083885.2:c.1462A>T	NP_001077354.2:p.Thr488Ser
NM_001173425.1:c.2608A>T	NP_001166896.1:p.Thr870Ser
NM_015404.3:c.2611A>T	NP_056219.3:p.Thr871Ser
XM_005251897.3:c.1948A>T	XP_005251954.2:p.Thr650Ser
XM_011518484.1:c.2644A>T	XP_011516786.1:p.Thr882Ser
XM_011518485.1:c.2644A>T	XP_011516787.1:p.Thr882Ser
XM_011518486.1:c.2641A>T	XP_011516788.1:p.Thr881Ser
XM_011518487.1:c.2518A>T	XP_011516789.1:p.Thr840Ser
XM_011518488.1:c.2401A>T	XP_011516790.1:p.Thr801Ser
XM_011518495.1:c.1321A>T	XP_011516797.1:p.Thr441Ser
NM_001346890.1:c.1558A>T	NP_001333819.1:p.Thr520Ser
XM_011518486.2:c.2641A>T	XP_011516788.1:p.Thr881Ser
XM_011518487.2:c.2518A>T	XP_011516789.1:p.Thr840Ser
XM_011518488.2:c.2401A>T	XP_011516790.1:p.Thr801Ser
NM_015404.4:c.2611A>T MANE Select	NP_056219.3:p.Thr871Ser
NM_001173425.2:c.2608A>T	NP_001166896.1:p.Thr870Ser
NM_001083885.3:c.1462A>T	NP_001077354.2:p.Thr488Ser