Canonical Allele Identifier: CA1873825876

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403966A= , CM000671.2:g.114403966A=	GRCh38
NC_000009.11:g.117166246A= , CM000671.1:g.117166246A=	GRCh37
NC_000009.10:g.116206067A=	NCBI36
NG_016700.1:g.106491T=

Transcript Alleles

HGVS	Amino-acid Change
NM_015404.4:c.2348T= MANE Select	NP_056219.3:p.Val783=
ENST00000362057.4:c.2348T= MANE Select	ENSP00000354623.3:p.Val783=
NM_001083885.2:c.1199T=	NP_001077354.2:p.Val400=
NM_001083885.3:c.1199T=	NP_001077354.2:p.Val400=
NM_001173425.1:c.2345T=	NP_001166896.1:p.Val782=
NM_001173425.2:c.2345T=	NP_001166896.1:p.Val782=
NM_001346890.1:c.1295T=	NP_001333819.1:p.Val432=
NM_015404.3:c.2348T=	NP_056219.3:p.Val783=
ENST00000265134.10:c.1199T=	ENSP00000265134.6:p.Val400=
ENST00000362057.3:c.2348T=	ENSP00000354623.3:p.Val783=
ENST00000374059.7:c.1295T=	ENSP00000363172.3:p.Val432=
ENST00000674036.8:c.1321T=
ENST00000674048.1:n.2229T=
ENST00000699485.1:c.692T=	ENSP00000514396.1:p.Val231=
XM_005251897.3:c.1685T=	XP_005251954.2:p.Val562=
XM_011518484.1:c.2381T=	XP_011516786.1:p.Val794=
XM_011518485.1:c.2381T=	XP_011516787.1:p.Val794=
XM_011518486.1:c.2378T=	XP_011516788.1:p.Val793=
XM_011518486.2:c.2378T=	XP_011516788.1:p.Val793=
XM_011518487.1:c.2255T=	XP_011516789.1:p.Val752=
XM_011518487.2:c.2255T=	XP_011516789.1:p.Val752=
XM_011518488.1:c.2138T=	XP_011516790.1:p.Val713=
XM_011518488.2:c.2138T=	XP_011516790.1:p.Val713=
XM_011518495.1:c.1058T=	XP_011516797.1:p.Val353=
XR_929747.1:n.3285T=
XR_929747.2:n.2596T=
XR_929748.1:n.3183T=
XR_929748.2:n.2494T=