Canonical Allele Identifier: CA1873825383

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402904G= , CM000671.2:g.114402904G=	GRCh38
NC_000009.11:g.117165184G= , CM000671.1:g.117165184G=	GRCh37
NC_000009.10:g.116205005G=	NCBI36
NG_016700.1:g.107553C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.918C=	ENSP00000514396.1:p.Leu306=
ENST00000362057.4:c.2574C= MANE Select	ENSP00000354623.3:p.Leu858=
ENST00000674036.8:c.1547C=
ENST00000674048.1:n.2455C=
ENST00000265134.10:c.1425C=	ENSP00000265134.6:p.Leu475=
ENST00000362057.3:c.2574C=	ENSP00000354623.3:p.Leu858=
ENST00000374059.7:c.1521C=	ENSP00000363172.3:p.Leu507=
NM_001083885.2:c.1425C=	NP_001077354.2:p.Leu475=
NM_001173425.1:c.2571C=	NP_001166896.1:p.Leu857=
NM_015404.3:c.2574C=	NP_056219.3:p.Leu858=
XM_005251897.3:c.1911C=	XP_005251954.2:p.Leu637=
XM_011518484.1:c.2607C=	XP_011516786.1:p.Leu869=
XM_011518485.1:c.2607C=	XP_011516787.1:p.Leu869=
XM_011518486.1:c.2604C=	XP_011516788.1:p.Leu868=
XM_011518487.1:c.2481C=	XP_011516789.1:p.Leu827=
XM_011518488.1:c.2364C=	XP_011516790.1:p.Leu788=
XM_011518495.1:c.1284C=	XP_011516797.1:p.Leu428=
XR_929747.1:n.3511C=
XR_929748.1:n.3409C=
NM_001346890.1:c.1521C=	NP_001333819.1:p.Leu507=
XM_011518486.2:c.2604C=	XP_011516788.1:p.Leu868=
XM_011518487.2:c.2481C=	XP_011516789.1:p.Leu827=
XM_011518488.2:c.2364C=	XP_011516790.1:p.Leu788=
XR_929747.2:n.2822C=
XR_929748.2:n.2720C=
NM_015404.4:c.2574C= MANE Select	NP_056219.3:p.Leu858=
NM_001173425.2:c.2571C=	NP_001166896.1:p.Leu857=
NM_001083885.3:c.1425C=	NP_001077354.2:p.Leu475=