Canonical Allele Identifier: CA1873825209

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402493C= , CM000671.2:g.114402493C=	GRCh38
NC_000009.11:g.117164773C= , CM000671.1:g.117164773C=	GRCh37
NC_000009.10:g.116204594C=	NCBI36
NG_016700.1:g.107964G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.1329G=	ENSP00000514396.1:n.1329G=
ENST00000362057.4:c.*261G= MANE Select	ENSP00000354623.3:n.*261G=
ENST00000674036.8:c.1958G=
ENST00000674048.1:n.2866G=
ENST00000265134.10:c.*261G=	ENSP00000265134.6:n.*261G=
ENST00000362057.3:c.*261G=	ENSP00000354623.3:n.*261G=
ENST00000374059.7:c.*261G=	ENSP00000363172.3:n.*261G=
NM_001083885.2:c.*261G=	NP_001077354.2:n.*261G=
NM_001173425.1:c.*261G=	NP_001166896.1:n.*261G=
NM_015404.3:c.*261G=	NP_056219.3:n.*261G=
XM_005251897.3:c.*261G=	XP_005251954.2:n.*261G=
XM_011518484.1:c.*261G=	XP_011516786.1:n.*261G=
XM_011518485.1:c.*261G=	XP_011516787.1:n.*261G=
XM_011518486.1:c.*261G=	XP_011516788.1:n.*261G=
XM_011518487.1:c.*261G=	XP_011516789.1:n.*261G=
XM_011518488.1:c.*261G=	XP_011516790.1:n.*261G=
XM_011518495.1:c.*261G=	XP_011516797.1:n.*261G=
NM_001346890.1:c.*261G=	NP_001333819.1:n.*261G=
XM_011518486.2:c.*261G=	XP_011516788.1:n.*261G=
XM_011518487.2:c.*261G=	XP_011516789.1:n.*261G=
XM_011518488.2:c.*261G=	XP_011516790.1:n.*261G=
NM_015404.4:c.*261G= MANE Select	NP_056219.3:n.*261G=
NM_001173425.2:c.*261G=	NP_001166896.1:n.*261G=
NM_001083885.3:c.*261G=	NP_001077354.2:n.*261G=