Canonical Allele Identifier: CA466782011

Gene: WHRN

Linked Data

• gnomAD v4: 9-114404043-C-T
• MyVariant Identifiers: chr9:g.117166323C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404043C>T , CM000671.2:g.114404043C>T	GRCh38
NC_000009.11:g.117166323C>T , CM000671.1:g.117166323C>T	GRCh37
NC_000009.10:g.116206144C>T	NCBI36
NG_016700.1:g.106414G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.615G>A	ENSP00000514396.1:p.Gly205=
ENST00000362057.4:c.2271G>A MANE Select	ENSP00000354623.3:p.Gly757=
ENST00000674036.8:c.1244G>A
ENST00000674048.1:n.2152G>A
ENST00000265134.10:c.1122G>A	ENSP00000265134.6:p.Gly374=
ENST00000362057.3:c.2271G>A	ENSP00000354623.3:p.Gly757=
ENST00000374059.7:c.1218G>A	ENSP00000363172.3:p.Gly406=
NM_001083885.2:c.1122G>A	NP_001077354.2:p.Gly374=
NM_001173425.1:c.2268G>A	NP_001166896.1:p.Gly756=
NM_015404.3:c.2271G>A	NP_056219.3:p.Gly757=
XM_005251897.3:c.1608G>A	XP_005251954.2:p.Gly536=
XM_011518484.1:c.2304G>A	XP_011516786.1:p.Gly768=
XM_011518485.1:c.2304G>A	XP_011516787.1:p.Gly768=
XM_011518486.1:c.2301G>A	XP_011516788.1:p.Gly767=
XM_011518487.1:c.2178G>A	XP_011516789.1:p.Gly726=
XM_011518488.1:c.2061G>A	XP_011516790.1:p.Gly687=
XM_011518495.1:c.981G>A	XP_011516797.1:p.Gly327=
XR_929747.1:n.3208G>A
XR_929748.1:n.3106G>A
NM_001346890.1:c.1218G>A	NP_001333819.1:p.Gly406=
XM_011518486.2:c.2301G>A	XP_011516788.1:p.Gly767=
XM_011518487.2:c.2178G>A	XP_011516789.1:p.Gly726=
XM_011518488.2:c.2061G>A	XP_011516790.1:p.Gly687=
XR_929747.2:n.2519G>A
XR_929748.2:n.2417G>A
NM_015404.4:c.2271G>A MANE Select	NP_056219.3:p.Gly757=
NM_001173425.2:c.2268G>A	NP_001166896.1:p.Gly756=
NM_001083885.3:c.1122G>A	NP_001077354.2:p.Gly374=