Canonical Allele Identifier: CA1873827859

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114407996G= , CM000671.2:g.114407996G=	GRCh38
NC_000009.11:g.117170276G= , CM000671.1:g.117170276G=	GRCh37
NC_000009.10:g.116210097G=	NCBI36
NG_016700.1:g.102461C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362057.4:c.1649C= MANE Select	ENSP00000354623.3:p.Thr550=
ENST00000673811.1:n.2373C=
ENST00000674036.8:c.622C=
ENST00000674048.1:n.1530C=
ENST00000265134.10:c.500C=	ENSP00000265134.6:p.Thr167=
ENST00000362057.3:c.1649C=	ENSP00000354623.3:p.Thr550=
ENST00000374059.7:c.596C=	ENSP00000363172.3:p.Thr199=
NM_001083885.2:c.500C=	NP_001077354.2:p.Thr167=
NM_001173425.1:c.1649C=	NP_001166896.1:p.Thr550=
NM_015404.3:c.1649C=	NP_056219.3:p.Thr550=
XM_005251897.3:c.986C=	XP_005251954.2:p.Thr329=
XM_011518484.1:c.1682C=	XP_011516786.1:p.Thr561=
XM_011518485.1:c.1682C=	XP_011516787.1:p.Thr561=
XM_011518486.1:c.1682C=	XP_011516788.1:p.Thr561=
XM_011518487.1:c.1556C=	XP_011516789.1:p.Thr519=
XM_011518488.1:c.1439C=	XP_011516790.1:p.Thr480=
XM_011518492.1:c.*34C=	XP_011516794.1:n.*34C=
XM_011518495.1:c.359C=	XP_011516797.1:p.Thr120=
XR_929747.1:n.2586C=
XR_929748.1:n.2484C=
XR_929750.1:n.2585C=
XR_929751.1:n.2492C=
XR_929757.1:n.2459C=
NM_001346890.1:c.596C=	NP_001333819.1:p.Thr199=
XM_011518486.2:c.1682C=	XP_011516788.1:p.Thr561=
XM_011518487.2:c.1556C=	XP_011516789.1:p.Thr519=
XM_011518488.2:c.1439C=	XP_011516790.1:p.Thr480=
XM_011518492.2:c.*34C=	XP_011516794.1:n.*34C=
XR_929747.2:n.1897C=
XR_929748.2:n.1795C=
XR_929750.3:n.1896C=
XR_929757.2:n.1770C=
NM_015404.4:c.1649C= MANE Select	NP_056219.3:p.Thr550=
NM_001173425.2:c.1649C=	NP_001166896.1:p.Thr550=
NM_001083885.3:c.500C=	NP_001077354.2:p.Thr167=