Canonical Allele Identifier: CA1873825219

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402528A= , CM000671.2:g.114402528A=	GRCh38
NC_000009.11:g.117164808A= , CM000671.1:g.117164808A=	GRCh37
NC_000009.10:g.116204629A=	NCBI36
NG_016700.1:g.107929T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1294T=	ENSP00000514396.1:n.1294T=
ENST00000362057.4:c.*226T= MANE Select	ENSP00000354623.3:n.*226T=
ENST00000674036.8:c.1923T=
ENST00000674048.1:n.2831T=
ENST00000265134.10:c.*226T=	ENSP00000265134.6:n.*226T=
ENST00000362057.3:c.*226T=	ENSP00000354623.3:n.*226T=
ENST00000374059.7:c.*226T=	ENSP00000363172.3:n.*226T=
NM_001083885.2:c.*226T=	NP_001077354.2:n.*226T=
NM_001173425.1:c.*226T=	NP_001166896.1:n.*226T=
NM_015404.3:c.*226T=	NP_056219.3:n.*226T=
XM_005251897.3:c.*226T=	XP_005251954.2:n.*226T=
XM_011518484.1:c.*226T=	XP_011516786.1:n.*226T=
XM_011518485.1:c.*226T=	XP_011516787.1:n.*226T=
XM_011518486.1:c.*226T=	XP_011516788.1:n.*226T=
XM_011518487.1:c.*226T=	XP_011516789.1:n.*226T=
XM_011518488.1:c.*226T=	XP_011516790.1:n.*226T=
XM_011518495.1:c.*226T=	XP_011516797.1:n.*226T=
NM_001346890.1:c.*226T=	NP_001333819.1:n.*226T=
XM_011518486.2:c.*226T=	XP_011516788.1:n.*226T=
XM_011518487.2:c.*226T=	XP_011516789.1:n.*226T=
XM_011518488.2:c.*226T=	XP_011516790.1:n.*226T=
NM_015404.4:c.*226T= MANE Select	NP_056219.3:n.*226T=
NM_001173425.2:c.*226T=	NP_001166896.1:n.*226T=
NM_001083885.3:c.*226T=	NP_001077354.2:n.*226T=