Canonical Allele Identifier: CA1873825373

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402870G= , CM000671.2:g.114402870G=	GRCh38
NC_000009.11:g.117165150G= , CM000671.1:g.117165150G=	GRCh37
NC_000009.10:g.116204971G=	NCBI36
NG_016700.1:g.107587C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.952C=	ENSP00000514396.1:p.Leu318=
ENST00000362057.4:c.2608C= MANE Select	ENSP00000354623.3:p.Leu870=
ENST00000674036.8:c.1581C=
ENST00000674048.1:n.2489C=
ENST00000265134.10:c.1459C=	ENSP00000265134.6:p.Leu487=
ENST00000362057.3:c.2608C=	ENSP00000354623.3:p.Leu870=
ENST00000374059.7:c.1555C=	ENSP00000363172.3:p.Leu519=
NM_001083885.2:c.1459C=	NP_001077354.2:p.Leu487=
NM_001173425.1:c.2605C=	NP_001166896.1:p.Leu869=
NM_015404.3:c.2608C=	NP_056219.3:p.Leu870=
XM_005251897.3:c.1945C=	XP_005251954.2:p.Leu649=
XM_011518484.1:c.2641C=	XP_011516786.1:p.Leu881=
XM_011518485.1:c.2641C=	XP_011516787.1:p.Leu881=
XM_011518486.1:c.2638C=	XP_011516788.1:p.Leu880=
XM_011518487.1:c.2515C=	XP_011516789.1:p.Leu839=
XM_011518488.1:c.2398C=	XP_011516790.1:p.Leu800=
XM_011518495.1:c.1318C=	XP_011516797.1:p.Leu440=
NM_001346890.1:c.1555C=	NP_001333819.1:p.Leu519=
XM_011518486.2:c.2638C=	XP_011516788.1:p.Leu880=
XM_011518487.2:c.2515C=	XP_011516789.1:p.Leu839=
XM_011518488.2:c.2398C=	XP_011516790.1:p.Leu800=
NM_015404.4:c.2608C= MANE Select	NP_056219.3:p.Leu870=
NM_001173425.2:c.2605C=	NP_001166896.1:p.Leu869=
NM_001083885.3:c.1459C=	NP_001077354.2:p.Leu487=