Canonical Allele Identifier: CA1873825353

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402837C= , CM000671.2:g.114402837C=	GRCh38
NC_000009.11:g.117165117C= , CM000671.1:g.117165117C=	GRCh37
NC_000009.10:g.116204938C=	NCBI36
NG_016700.1:g.107620G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.985G=	ENSP00000514396.1:p.Ala329=
ENST00000362057.4:c.2641G= MANE Select	ENSP00000354623.3:p.Ala881=
ENST00000674036.8:c.1614G=
ENST00000674048.1:n.2522G=
ENST00000265134.10:c.1492G=	ENSP00000265134.6:p.Ala498=
ENST00000362057.3:c.2641G=	ENSP00000354623.3:p.Ala881=
ENST00000374059.7:c.1588G=	ENSP00000363172.3:p.Ala530=
NM_001083885.2:c.1492G=	NP_001077354.2:p.Ala498=
NM_001173425.1:c.2638G=	NP_001166896.1:p.Ala880=
NM_015404.3:c.2641G=	NP_056219.3:p.Ala881=
XM_005251897.3:c.1978G=	XP_005251954.2:p.Ala660=
XM_011518484.1:c.2674G=	XP_011516786.1:p.Ala892=
XM_011518485.1:c.2674G=	XP_011516787.1:p.Ala892=
XM_011518486.1:c.2671G=	XP_011516788.1:p.Ala891=
XM_011518487.1:c.2548G=	XP_011516789.1:p.Ala850=
XM_011518488.1:c.2431G=	XP_011516790.1:p.Ala811=
XM_011518495.1:c.1351G=	XP_011516797.1:p.Ala451=
NM_001346890.1:c.1588G=	NP_001333819.1:p.Ala530=
XM_011518486.2:c.2671G=	XP_011516788.1:p.Ala891=
XM_011518487.2:c.2548G=	XP_011516789.1:p.Ala850=
XM_011518488.2:c.2431G=	XP_011516790.1:p.Ala811=
NM_015404.4:c.2641G= MANE Select	NP_056219.3:p.Ala881=
NM_001173425.2:c.2638G=	NP_001166896.1:p.Ala880=
NM_001083885.3:c.1492G=	NP_001077354.2:p.Ala498=