Canonical Allele Identifier: CA374618755

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165049G>C (hg19) ; chr9:g.114402769G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402769G>C , CM000671.2:g.114402769G>C	GRCh38
NC_000009.11:g.117165049G>C , CM000671.1:g.117165049G>C	GRCh37
NC_000009.10:g.116204870G>C	NCBI36
NG_016700.1:g.107688C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1053C>G	ENSP00000514396.1:p.Phe351Leu
ENST00000362057.4:c.2709C>G MANE Select	ENSP00000354623.3:p.Phe903Leu
ENST00000674036.8:c.1682C>G
ENST00000674048.1:n.2590C>G
ENST00000265134.10:c.1560C>G	ENSP00000265134.6:p.Phe520Leu
ENST00000362057.3:c.2709C>G	ENSP00000354623.3:p.Phe903Leu
ENST00000374059.7:c.1656C>G	ENSP00000363172.3:p.Phe552Leu
NM_001083885.2:c.1560C>G	NP_001077354.2:p.Phe520Leu
NM_001173425.1:c.2706C>G	NP_001166896.1:p.Phe902Leu
NM_015404.3:c.2709C>G	NP_056219.3:p.Phe903Leu
XM_005251897.3:c.2046C>G	XP_005251954.2:p.Phe682Leu
XM_011518484.1:c.2742C>G	XP_011516786.1:p.Phe914Leu
XM_011518485.1:c.2742C>G	XP_011516787.1:p.Phe914Leu
XM_011518486.1:c.2739C>G	XP_011516788.1:p.Phe913Leu
XM_011518487.1:c.2616C>G	XP_011516789.1:p.Phe872Leu
XM_011518488.1:c.2499C>G	XP_011516790.1:p.Phe833Leu
XM_011518495.1:c.1419C>G	XP_011516797.1:p.Phe473Leu
NM_001346890.1:c.1656C>G	NP_001333819.1:p.Phe552Leu
XM_011518486.2:c.2739C>G	XP_011516788.1:p.Phe913Leu
XM_011518487.2:c.2616C>G	XP_011516789.1:p.Phe872Leu
XM_011518488.2:c.2499C>G	XP_011516790.1:p.Phe833Leu
NM_015404.4:c.2709C>G MANE Select	NP_056219.3:p.Phe903Leu
NM_001173425.2:c.2706C>G	NP_001166896.1:p.Phe902Leu
NM_001083885.3:c.1560C>G	NP_001077354.2:p.Phe520Leu