Canonical Allele Identifier: CA1873825888

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403982G= , CM000671.2:g.114403982G=	GRCh38
NC_000009.11:g.117166262G= , CM000671.1:g.117166262G=	GRCh37
NC_000009.10:g.116206083G=	NCBI36
NG_016700.1:g.106475C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015404.4:c.2332C= MANE Select	NP_056219.3:p.Arg778=
ENST00000362057.4:c.2332C= MANE Select	ENSP00000354623.3:p.Arg778=
NM_001083885.2:c.1183C=	NP_001077354.2:p.Arg395=
NM_001083885.3:c.1183C=	NP_001077354.2:p.Arg395=
NM_001173425.1:c.2329C=	NP_001166896.1:p.Arg777=
NM_001173425.2:c.2329C=	NP_001166896.1:p.Arg777=
NM_001346890.1:c.1279C=	NP_001333819.1:p.Arg427=
NM_015404.3:c.2332C=	NP_056219.3:p.Arg778=
ENST00000265134.10:c.1183C=	ENSP00000265134.6:p.Arg395=
ENST00000362057.3:c.2332C=	ENSP00000354623.3:p.Arg778=
ENST00000374059.7:c.1279C=	ENSP00000363172.3:p.Arg427=
ENST00000674036.8:c.1305C=
ENST00000674048.1:n.2213C=
ENST00000699485.1:c.676C=	ENSP00000514396.1:p.Arg226=
XM_005251897.3:c.1669C=	XP_005251954.2:p.Arg557=
XM_011518484.1:c.2365C=	XP_011516786.1:p.Arg789=
XM_011518485.1:c.2365C=	XP_011516787.1:p.Arg789=
XM_011518486.1:c.2362C=	XP_011516788.1:p.Arg788=
XM_011518486.2:c.2362C=	XP_011516788.1:p.Arg788=
XM_011518487.1:c.2239C=	XP_011516789.1:p.Arg747=
XM_011518487.2:c.2239C=	XP_011516789.1:p.Arg747=
XM_011518488.1:c.2122C=	XP_011516790.1:p.Arg708=
XM_011518488.2:c.2122C=	XP_011516790.1:p.Arg708=
XM_011518495.1:c.1042C=	XP_011516797.1:p.Arg348=
XR_929747.1:n.3269C=
XR_929747.2:n.2580C=
XR_929748.1:n.3167C=
XR_929748.2:n.2478C=