Canonical Allele Identifier: CA1873827121

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406511C= , CM000671.2:g.114406511C=	GRCh38
NC_000009.11:g.117168791C= , CM000671.1:g.117168791C=	GRCh37
NC_000009.10:g.116208612C=	NCBI36
NG_016700.1:g.103946G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.424G=	ENSP00000514396.1:p.Ala142=
ENST00000362057.4:c.2080G= MANE Select	ENSP00000354623.3:p.Ala694=
ENST00000674036.8:c.1053G=
ENST00000674048.1:n.1961G=
ENST00000265134.10:c.931G=	ENSP00000265134.6:p.Ala311=
ENST00000362057.3:c.2080G=	ENSP00000354623.3:p.Ala694=
ENST00000374059.7:c.1027G=	ENSP00000363172.3:p.Ala343=
NM_001083885.2:c.931G=	NP_001077354.2:p.Ala311=
NM_001173425.1:c.2080G=	NP_001166896.1:p.Ala694=
NM_015404.3:c.2080G=	NP_056219.3:p.Ala694=
XM_005251897.3:c.1417G=	XP_005251954.2:p.Ala473=
XM_011518484.1:c.2113G=	XP_011516786.1:p.Ala705=
XM_011518485.1:c.2113G=	XP_011516787.1:p.Ala705=
XM_011518486.1:c.2113G=	XP_011516788.1:p.Ala705=
XM_011518487.1:c.1987G=	XP_011516789.1:p.Ala663=
XM_011518488.1:c.1870G=	XP_011516790.1:p.Ala624=
XM_011518495.1:c.790G=	XP_011516797.1:p.Ala264=
XR_929747.1:n.3017G=
XR_929748.1:n.2915G=
NM_001346890.1:c.1027G=	NP_001333819.1:p.Ala343=
XM_011518486.2:c.2113G=	XP_011516788.1:p.Ala705=
XM_011518487.2:c.1987G=	XP_011516789.1:p.Ala663=
XM_011518488.2:c.1870G=	XP_011516790.1:p.Ala624=
XR_929747.2:n.2328G=
XR_929748.2:n.2226G=
NM_015404.4:c.2080G= MANE Select	NP_056219.3:p.Ala694=
NM_001173425.2:c.2080G=	NP_001166896.1:p.Ala694=
NM_001083885.3:c.931G=	NP_001077354.2:p.Ala311=