Canonical Allele Identifier: CA1873827119

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406506C= , CM000671.2:g.114406506C=	GRCh38
NC_000009.11:g.117168786C= , CM000671.1:g.117168786C=	GRCh37
NC_000009.10:g.116208607C=	NCBI36
NG_016700.1:g.103951G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.429G=	ENSP00000514396.1:p.Glu143=
ENST00000362057.4:c.2085G= MANE Select	ENSP00000354623.3:p.Glu695=
ENST00000674036.8:c.1058G=
ENST00000674048.1:n.1966G=
ENST00000265134.10:c.936G=	ENSP00000265134.6:p.Glu312=
ENST00000362057.3:c.2085G=	ENSP00000354623.3:p.Glu695=
ENST00000374059.7:c.1032G=	ENSP00000363172.3:p.Glu344=
NM_001083885.2:c.936G=	NP_001077354.2:p.Glu312=
NM_001173425.1:c.2085G=	NP_001166896.1:p.Glu695=
NM_015404.3:c.2085G=	NP_056219.3:p.Glu695=
XM_005251897.3:c.1422G=	XP_005251954.2:p.Glu474=
XM_011518484.1:c.2118G=	XP_011516786.1:p.Glu706=
XM_011518485.1:c.2118G=	XP_011516787.1:p.Glu706=
XM_011518486.1:c.2118G=	XP_011516788.1:p.Glu706=
XM_011518487.1:c.1992G=	XP_011516789.1:p.Glu664=
XM_011518488.1:c.1875G=	XP_011516790.1:p.Glu625=
XM_011518495.1:c.795G=	XP_011516797.1:p.Glu265=
XR_929747.1:n.3022G=
XR_929748.1:n.2920G=
NM_001346890.1:c.1032G=	NP_001333819.1:p.Glu344=
XM_011518486.2:c.2118G=	XP_011516788.1:p.Glu706=
XM_011518487.2:c.1992G=	XP_011516789.1:p.Glu664=
XM_011518488.2:c.1875G=	XP_011516790.1:p.Glu625=
XR_929747.2:n.2333G=
XR_929748.2:n.2231G=
NM_015404.4:c.2085G= MANE Select	NP_056219.3:p.Glu695=
NM_001173425.2:c.2085G=	NP_001166896.1:p.Glu695=
NM_001083885.3:c.936G=	NP_001077354.2:p.Glu312=