Canonical Allele Identifier: CA1873827860

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114407998T= , CM000671.2:g.114407998T=	GRCh38
NC_000009.11:g.117170278T= , CM000671.1:g.117170278T=	GRCh37
NC_000009.10:g.116210099T=	NCBI36
NG_016700.1:g.102459A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362057.4:c.1647A= MANE Select	ENSP00000354623.3:p.Glu549=
ENST00000673811.1:n.2371A=
ENST00000674036.8:c.620A=
ENST00000674048.1:n.1528A=
ENST00000265134.10:c.498A=	ENSP00000265134.6:p.Glu166=
ENST00000362057.3:c.1647A=	ENSP00000354623.3:p.Glu549=
ENST00000374059.7:c.594A=	ENSP00000363172.3:p.Glu198=
NM_001083885.2:c.498A=	NP_001077354.2:p.Glu166=
NM_001173425.1:c.1647A=	NP_001166896.1:p.Glu549=
NM_015404.3:c.1647A=	NP_056219.3:p.Glu549=
XM_005251897.3:c.984A=	XP_005251954.2:p.Glu328=
XM_011518484.1:c.1680A=	XP_011516786.1:p.Glu560=
XM_011518485.1:c.1680A=	XP_011516787.1:p.Glu560=
XM_011518486.1:c.1680A=	XP_011516788.1:p.Glu560=
XM_011518487.1:c.1554A=	XP_011516789.1:p.Glu518=
XM_011518488.1:c.1437A=	XP_011516790.1:p.Glu479=
XM_011518492.1:c.*32A=	XP_011516794.1:n.*32A=
XM_011518495.1:c.357A=	XP_011516797.1:p.Glu119=
XR_929747.1:n.2584A=
XR_929748.1:n.2482A=
XR_929750.1:n.2583A=
XR_929751.1:n.2490A=
XR_929757.1:n.2457A=
NM_001346890.1:c.594A=	NP_001333819.1:p.Glu198=
XM_011518486.2:c.1680A=	XP_011516788.1:p.Glu560=
XM_011518487.2:c.1554A=	XP_011516789.1:p.Glu518=
XM_011518488.2:c.1437A=	XP_011516790.1:p.Glu479=
XM_011518492.2:c.*32A=	XP_011516794.1:n.*32A=
XR_929747.2:n.1895A=
XR_929748.2:n.1793A=
XR_929750.3:n.1894A=
XR_929757.2:n.1768A=
NM_015404.4:c.1647A= MANE Select	NP_056219.3:p.Glu549=
NM_001173425.2:c.1647A=	NP_001166896.1:p.Glu549=
NM_001083885.3:c.498A=	NP_001077354.2:p.Glu166=