Canonical Allele Identifier: CA374618909

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165122T>C (hg19) ; chr9:g.114402842T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402842T>C , CM000671.2:g.114402842T>C	GRCh38
NC_000009.11:g.117165122T>C , CM000671.1:g.117165122T>C	GRCh37
NC_000009.10:g.116204943T>C	NCBI36
NG_016700.1:g.107615A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.980A>G	ENSP00000514396.1:p.Glu327Gly
ENST00000362057.4:c.2636A>G MANE Select	ENSP00000354623.3:p.Glu879Gly
ENST00000674036.8:c.1609A>G
ENST00000674048.1:n.2517A>G
ENST00000265134.10:c.1487A>G	ENSP00000265134.6:p.Glu496Gly
ENST00000362057.3:c.2636A>G	ENSP00000354623.3:p.Glu879Gly
ENST00000374059.7:c.1583A>G	ENSP00000363172.3:p.Glu528Gly
NM_001083885.2:c.1487A>G	NP_001077354.2:p.Glu496Gly
NM_001173425.1:c.2633A>G	NP_001166896.1:p.Glu878Gly
NM_015404.3:c.2636A>G	NP_056219.3:p.Glu879Gly
XM_005251897.3:c.1973A>G	XP_005251954.2:p.Glu658Gly
XM_011518484.1:c.2669A>G	XP_011516786.1:p.Glu890Gly
XM_011518485.1:c.2669A>G	XP_011516787.1:p.Glu890Gly
XM_011518486.1:c.2666A>G	XP_011516788.1:p.Glu889Gly
XM_011518487.1:c.2543A>G	XP_011516789.1:p.Glu848Gly
XM_011518488.1:c.2426A>G	XP_011516790.1:p.Glu809Gly
XM_011518495.1:c.1346A>G	XP_011516797.1:p.Glu449Gly
NM_001346890.1:c.1583A>G	NP_001333819.1:p.Glu528Gly
XM_011518486.2:c.2666A>G	XP_011516788.1:p.Glu889Gly
XM_011518487.2:c.2543A>G	XP_011516789.1:p.Glu848Gly
XM_011518488.2:c.2426A>G	XP_011516790.1:p.Glu809Gly
NM_015404.4:c.2636A>G MANE Select	NP_056219.3:p.Glu879Gly
NM_001173425.2:c.2633A>G	NP_001166896.1:p.Glu878Gly
NM_001083885.3:c.1487A>G	NP_001077354.2:p.Glu496Gly