Canonical Allele Identifier: CA1873825850

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403926G= , CM000671.2:g.114403926G=	GRCh38
NC_000009.11:g.117166206G= , CM000671.1:g.117166206G=	GRCh37
NC_000009.10:g.116206027G=	NCBI36
NG_016700.1:g.106531C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.732C=	ENSP00000514396.1:p.Asn244=
ENST00000362057.4:c.2388C= MANE Select	ENSP00000354623.3:p.Asn796=
ENST00000674036.8:c.1361C=
ENST00000674048.1:n.2269C=
ENST00000265134.10:c.1239C=	ENSP00000265134.6:p.Asn413=
ENST00000362057.3:c.2388C=	ENSP00000354623.3:p.Asn796=
ENST00000374059.7:c.1335C=	ENSP00000363172.3:p.Asn445=
NM_001083885.2:c.1239C=	NP_001077354.2:p.Asn413=
NM_001173425.1:c.2385C=	NP_001166896.1:p.Asn795=
NM_015404.3:c.2388C=	NP_056219.3:p.Asn796=
XM_005251897.3:c.1725C=	XP_005251954.2:p.Asn575=
XM_011518484.1:c.2421C=	XP_011516786.1:p.Asn807=
XM_011518485.1:c.2421C=	XP_011516787.1:p.Asn807=
XM_011518486.1:c.2418C=	XP_011516788.1:p.Asn806=
XM_011518487.1:c.2295C=	XP_011516789.1:p.Asn765=
XM_011518488.1:c.2178C=	XP_011516790.1:p.Asn726=
XM_011518495.1:c.1098C=	XP_011516797.1:p.Asn366=
XR_929747.1:n.3325C=
XR_929748.1:n.3223C=
NM_001346890.1:c.1335C=	NP_001333819.1:p.Asn445=
XM_011518486.2:c.2418C=	XP_011516788.1:p.Asn806=
XM_011518487.2:c.2295C=	XP_011516789.1:p.Asn765=
XM_011518488.2:c.2178C=	XP_011516790.1:p.Asn726=
XR_929747.2:n.2636C=
XR_929748.2:n.2534C=
NM_015404.4:c.2388C= MANE Select	NP_056219.3:p.Asn796=
NM_001173425.2:c.2385C=	NP_001166896.1:p.Asn795=
NM_001083885.3:c.1239C=	NP_001077354.2:p.Asn413=