Canonical Allele Identifier: CA466911095

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165211G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402931G>C , CM000671.2:g.114402931G>C	GRCh38
NC_000009.11:g.117165211G>C , CM000671.1:g.117165211G>C	GRCh37
NC_000009.10:g.116205032G>C	NCBI36
NG_016700.1:g.107526C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.891C>G	ENSP00000514396.1:p.Gly297=
ENST00000362057.4:c.2547C>G MANE Select	ENSP00000354623.3:p.Gly849=
ENST00000674036.8:c.1520C>G
ENST00000674048.1:n.2428C>G
ENST00000265134.10:c.1398C>G	ENSP00000265134.6:p.Gly466=
ENST00000362057.3:c.2547C>G	ENSP00000354623.3:p.Gly849=
ENST00000374059.7:c.1494C>G	ENSP00000363172.3:p.Gly498=
NM_001083885.2:c.1398C>G	NP_001077354.2:p.Gly466=
NM_001173425.1:c.2544C>G	NP_001166896.1:p.Gly848=
NM_015404.3:c.2547C>G	NP_056219.3:p.Gly849=
XM_005251897.3:c.1884C>G	XP_005251954.2:p.Gly628=
XM_011518484.1:c.2580C>G	XP_011516786.1:p.Gly860=
XM_011518485.1:c.2580C>G	XP_011516787.1:p.Gly860=
XM_011518486.1:c.2577C>G	XP_011516788.1:p.Gly859=
XM_011518487.1:c.2454C>G	XP_011516789.1:p.Gly818=
XM_011518488.1:c.2337C>G	XP_011516790.1:p.Gly779=
XM_011518495.1:c.1257C>G	XP_011516797.1:p.Gly419=
XR_929747.1:n.3484C>G
XR_929748.1:n.3382C>G
NM_001346890.1:c.1494C>G	NP_001333819.1:p.Gly498=
XM_011518486.2:c.2577C>G	XP_011516788.1:p.Gly859=
XM_011518487.2:c.2454C>G	XP_011516789.1:p.Gly818=
XM_011518488.2:c.2337C>G	XP_011516790.1:p.Gly779=
XR_929747.2:n.2795C>G
XR_929748.2:n.2693C>G
NM_015404.4:c.2547C>G MANE Select	NP_056219.3:p.Gly849=
NM_001173425.2:c.2544C>G	NP_001166896.1:p.Gly848=
NM_001083885.3:c.1398C>G	NP_001077354.2:p.Gly466=