Canonical Allele Identifier: CA374620332

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117168787T>A (hg19) ; chr9:g.114406507T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406507T>A , CM000671.2:g.114406507T>A	GRCh38
NC_000009.11:g.117168787T>A , CM000671.1:g.117168787T>A	GRCh37
NC_000009.10:g.116208608T>A	NCBI36
NG_016700.1:g.103950A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.428A>T	ENSP00000514396.1:p.Glu143Val
ENST00000362057.4:c.2084A>T MANE Select	ENSP00000354623.3:p.Glu695Val
ENST00000674036.8:c.1057A>T
ENST00000674048.1:n.1965A>T
ENST00000265134.10:c.935A>T	ENSP00000265134.6:p.Glu312Val
ENST00000362057.3:c.2084A>T	ENSP00000354623.3:p.Glu695Val
ENST00000374059.7:c.1031A>T	ENSP00000363172.3:p.Glu344Val
NM_001083885.2:c.935A>T	NP_001077354.2:p.Glu312Val
NM_001173425.1:c.2084A>T	NP_001166896.1:p.Glu695Val
NM_015404.3:c.2084A>T	NP_056219.3:p.Glu695Val
XM_005251897.3:c.1421A>T	XP_005251954.2:p.Glu474Val
XM_011518484.1:c.2117A>T	XP_011516786.1:p.Glu706Val
XM_011518485.1:c.2117A>T	XP_011516787.1:p.Glu706Val
XM_011518486.1:c.2117A>T	XP_011516788.1:p.Glu706Val
XM_011518487.1:c.1991A>T	XP_011516789.1:p.Glu664Val
XM_011518488.1:c.1874A>T	XP_011516790.1:p.Glu625Val
XM_011518495.1:c.794A>T	XP_011516797.1:p.Glu265Val
XR_929747.1:n.3021A>T
XR_929748.1:n.2919A>T
NM_001346890.1:c.1031A>T	NP_001333819.1:p.Glu344Val
XM_011518486.2:c.2117A>T	XP_011516788.1:p.Glu706Val
XM_011518487.2:c.1991A>T	XP_011516789.1:p.Glu664Val
XM_011518488.2:c.1874A>T	XP_011516790.1:p.Glu625Val
XR_929747.2:n.2332A>T
XR_929748.2:n.2230A>T
NM_015404.4:c.2084A>T MANE Select	NP_056219.3:p.Glu695Val
NM_001173425.2:c.2084A>T	NP_001166896.1:p.Glu695Val
NM_001083885.3:c.935A>T	NP_001077354.2:p.Glu312Val