Canonical Allele Identifier: CA374619951

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117166330T>A (hg19) ; chr9:g.114404050T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404050T>A , CM000671.2:g.114404050T>A	GRCh38
NC_000009.11:g.117166330T>A , CM000671.1:g.117166330T>A	GRCh37
NC_000009.10:g.116206151T>A	NCBI36
NG_016700.1:g.106407A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.608A>T	ENSP00000514396.1:p.Asp203Val
ENST00000362057.4:c.2264A>T MANE Select	ENSP00000354623.3:p.Asp755Val
ENST00000674036.8:c.1237A>T
ENST00000674048.1:n.2145A>T
ENST00000265134.10:c.1115A>T	ENSP00000265134.6:p.Asp372Val
ENST00000362057.3:c.2264A>T	ENSP00000354623.3:p.Asp755Val
ENST00000374059.7:c.1211A>T	ENSP00000363172.3:p.Asp404Val
NM_001083885.2:c.1115A>T	NP_001077354.2:p.Asp372Val
NM_001173425.1:c.2261A>T	NP_001166896.1:p.Asp754Val
NM_015404.3:c.2264A>T	NP_056219.3:p.Asp755Val
XM_005251897.3:c.1601A>T	XP_005251954.2:p.Asp534Val
XM_011518484.1:c.2297A>T	XP_011516786.1:p.Asp766Val
XM_011518485.1:c.2297A>T	XP_011516787.1:p.Asp766Val
XM_011518486.1:c.2294A>T	XP_011516788.1:p.Asp765Val
XM_011518487.1:c.2171A>T	XP_011516789.1:p.Asp724Val
XM_011518488.1:c.2054A>T	XP_011516790.1:p.Asp685Val
XM_011518495.1:c.974A>T	XP_011516797.1:p.Asp325Val
XR_929747.1:n.3201A>T
XR_929748.1:n.3099A>T
NM_001346890.1:c.1211A>T	NP_001333819.1:p.Asp404Val
XM_011518486.2:c.2294A>T	XP_011516788.1:p.Asp765Val
XM_011518487.2:c.2171A>T	XP_011516789.1:p.Asp724Val
XM_011518488.2:c.2054A>T	XP_011516790.1:p.Asp685Val
XR_929747.2:n.2512A>T
XR_929748.2:n.2410A>T
NM_015404.4:c.2264A>T MANE Select	NP_056219.3:p.Asp755Val
NM_001173425.2:c.2261A>T	NP_001166896.1:p.Asp754Val
NM_001083885.3:c.1115A>T	NP_001077354.2:p.Asp372Val