Canonical Allele Identifier: CA1873827127

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406521T= , CM000671.2:g.114406521T=	GRCh38
NC_000009.11:g.117168801T= , CM000671.1:g.117168801T=	GRCh37
NC_000009.10:g.116208622T=	NCBI36
NG_016700.1:g.103936A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.414A=	ENSP00000514396.1:p.Lys138=
ENST00000362057.4:c.2070A= MANE Select	ENSP00000354623.3:p.Lys690=
ENST00000674036.8:c.1043A=
ENST00000674048.1:n.1951A=
ENST00000265134.10:c.921A=	ENSP00000265134.6:p.Lys307=
ENST00000362057.3:c.2070A=	ENSP00000354623.3:p.Lys690=
ENST00000374059.7:c.1017A=	ENSP00000363172.3:p.Lys339=
NM_001083885.2:c.921A=	NP_001077354.2:p.Lys307=
NM_001173425.1:c.2070A=	NP_001166896.1:p.Lys690=
NM_015404.3:c.2070A=	NP_056219.3:p.Lys690=
XM_005251897.3:c.1407A=	XP_005251954.2:p.Lys469=
XM_011518484.1:c.2103A=	XP_011516786.1:p.Lys701=
XM_011518485.1:c.2103A=	XP_011516787.1:p.Lys701=
XM_011518486.1:c.2103A=	XP_011516788.1:p.Lys701=
XM_011518487.1:c.1977A=	XP_011516789.1:p.Lys659=
XM_011518488.1:c.1860A=	XP_011516790.1:p.Lys620=
XM_011518495.1:c.780A=	XP_011516797.1:p.Lys260=
XR_929747.1:n.3007A=
XR_929748.1:n.2905A=
NM_001346890.1:c.1017A=	NP_001333819.1:p.Lys339=
XM_011518486.2:c.2103A=	XP_011516788.1:p.Lys701=
XM_011518487.2:c.1977A=	XP_011516789.1:p.Lys659=
XM_011518488.2:c.1860A=	XP_011516790.1:p.Lys620=
XR_929747.2:n.2318A=
XR_929748.2:n.2216A=
NM_015404.4:c.2070A= MANE Select	NP_056219.3:p.Lys690=
NM_001173425.2:c.2070A=	NP_001166896.1:p.Lys690=
NM_001083885.3:c.921A=	NP_001077354.2:p.Lys307=