Canonical Allele Identifier: CA1873827851

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114407985C= , CM000671.2:g.114407985C=	GRCh38
NC_000009.11:g.117170265C= , CM000671.1:g.117170265C=	GRCh37
NC_000009.10:g.116210086C=	NCBI36
NG_016700.1:g.102472G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362057.4:c.1660G= MANE Select	ENSP00000354623.3:p.Val554=
ENST00000673811.1:n.2384G=
ENST00000674036.8:c.633G=
ENST00000674048.1:n.1541G=
ENST00000265134.10:c.511G=	ENSP00000265134.6:p.Val171=
ENST00000362057.3:c.1660G=	ENSP00000354623.3:p.Val554=
ENST00000374059.7:c.607G=	ENSP00000363172.3:p.Val203=
NM_001083885.2:c.511G=	NP_001077354.2:p.Val171=
NM_001173425.1:c.1660G=	NP_001166896.1:p.Val554=
NM_015404.3:c.1660G=	NP_056219.3:p.Val554=
XM_005251897.3:c.997G=	XP_005251954.2:p.Val333=
XM_011518484.1:c.1693G=	XP_011516786.1:p.Val565=
XM_011518485.1:c.1693G=	XP_011516787.1:p.Val565=
XM_011518486.1:c.1693G=	XP_011516788.1:p.Val565=
XM_011518487.1:c.1567G=	XP_011516789.1:p.Val523=
XM_011518488.1:c.1450G=	XP_011516790.1:p.Val484=
XM_011518492.1:c.*45G=	XP_011516794.1:n.*45G=
XM_011518495.1:c.370G=	XP_011516797.1:p.Val124=
XR_929747.1:n.2597G=
XR_929748.1:n.2495G=
XR_929750.1:n.2596G=
XR_929751.1:n.2503G=
XR_929757.1:n.2470G=
NM_001346890.1:c.607G=	NP_001333819.1:p.Val203=
XM_011518486.2:c.1693G=	XP_011516788.1:p.Val565=
XM_011518487.2:c.1567G=	XP_011516789.1:p.Val523=
XM_011518488.2:c.1450G=	XP_011516790.1:p.Val484=
XM_011518492.2:c.*45G=	XP_011516794.1:n.*45G=
XR_929747.2:n.1908G=
XR_929748.2:n.1806G=
XR_929750.3:n.1907G=
XR_929757.2:n.1781G=
NM_015404.4:c.1660G= MANE Select	NP_056219.3:p.Val554=
NM_001173425.2:c.1660G=	NP_001166896.1:p.Val554=
NM_001083885.3:c.511G=	NP_001077354.2:p.Val171=