Canonical Allele Identifier: CA1873825341

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402812T= , CM000671.2:g.114402812T=	GRCh38
NC_000009.11:g.117165092T= , CM000671.1:g.117165092T=	GRCh37
NC_000009.10:g.116204913T=	NCBI36
NG_016700.1:g.107645A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1010A=	ENSP00000514396.1:p.Lys337=
ENST00000362057.4:c.2666A= MANE Select	ENSP00000354623.3:p.Lys889=
ENST00000674036.8:c.1639A=
ENST00000674048.1:n.2547A=
ENST00000265134.10:c.1517A=	ENSP00000265134.6:p.Lys506=
ENST00000362057.3:c.2666A=	ENSP00000354623.3:p.Lys889=
ENST00000374059.7:c.1613A=	ENSP00000363172.3:p.Lys538=
NM_001083885.2:c.1517A=	NP_001077354.2:p.Lys506=
NM_001173425.1:c.2663A=	NP_001166896.1:p.Lys888=
NM_015404.3:c.2666A=	NP_056219.3:p.Lys889=
XM_005251897.3:c.2003A=	XP_005251954.2:p.Lys668=
XM_011518484.1:c.2699A=	XP_011516786.1:p.Lys900=
XM_011518485.1:c.2699A=	XP_011516787.1:p.Lys900=
XM_011518486.1:c.2696A=	XP_011516788.1:p.Lys899=
XM_011518487.1:c.2573A=	XP_011516789.1:p.Lys858=
XM_011518488.1:c.2456A=	XP_011516790.1:p.Lys819=
XM_011518495.1:c.1376A=	XP_011516797.1:p.Lys459=
NM_001346890.1:c.1613A=	NP_001333819.1:p.Lys538=
XM_011518486.2:c.2696A=	XP_011516788.1:p.Lys899=
XM_011518487.2:c.2573A=	XP_011516789.1:p.Lys858=
XM_011518488.2:c.2456A=	XP_011516790.1:p.Lys819=
NM_015404.4:c.2666A= MANE Select	NP_056219.3:p.Lys889=
NM_001173425.2:c.2663A=	NP_001166896.1:p.Lys888=
NM_001083885.3:c.1517A=	NP_001077354.2:p.Lys506=