Canonical Allele Identifier: CA858984397

Gene: WHRN

Linked Data

• dbSNP Id: rs1416815440
• gnomAD v2: 9-117164648-C-T
• gnomAD v3: 9-114402368-C-T
• gnomAD v4: 9-114402368-C-T
• MyVariant Identifiers: chr9:g.117164648C>T (hg19) ; chr9:g.114402368C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402368C>T , CM000671.2:g.114402368C>T	GRCh38
NC_000009.11:g.117164648C>T , CM000671.1:g.117164648C>T	GRCh37
NC_000009.10:g.116204469C>T	NCBI36
NG_016700.1:g.108089G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1454G>A	ENSP00000514396.1:n.1454G>A
ENST00000362057.4:c.*386G>A MANE Select	ENSP00000354623.3:n.*386G>A
ENST00000674036.8:c.2083G>A
ENST00000674048.1:n.2991G>A
ENST00000265134.10:c.*386G>A	ENSP00000265134.6:n.*386G>A
ENST00000362057.3:c.*386G>A	ENSP00000354623.3:n.*386G>A
ENST00000374059.7:c.*386G>A	ENSP00000363172.3:n.*386G>A
NM_001083885.2:c.*386G>A	NP_001077354.2:n.*386G>A
NM_001173425.1:c.*386G>A	NP_001166896.1:n.*386G>A
NM_015404.3:c.*386G>A	NP_056219.3:n.*386G>A
XM_005251897.3:c.*386G>A	XP_005251954.2:n.*386G>A
XM_011518484.1:c.*386G>A	XP_011516786.1:n.*386G>A
XM_011518485.1:c.*386G>A	XP_011516787.1:n.*386G>A
XM_011518486.1:c.*386G>A	XP_011516788.1:n.*386G>A
XM_011518487.1:c.*386G>A	XP_011516789.1:n.*386G>A
XM_011518488.1:c.*386G>A	XP_011516790.1:n.*386G>A
XM_011518495.1:c.*386G>A	XP_011516797.1:n.*386G>A
NM_001346890.1:c.*386G>A	NP_001333819.1:n.*386G>A
XM_011518486.2:c.*386G>A	XP_011516788.1:n.*386G>A
XM_011518487.2:c.*386G>A	XP_011516789.1:n.*386G>A
XM_011518488.2:c.*386G>A	XP_011516790.1:n.*386G>A
NM_015404.4:c.*386G>A MANE Select	NP_056219.3:n.*386G>A
NM_001173425.2:c.*386G>A	NP_001166896.1:n.*386G>A
NM_001083885.3:c.*386G>A	NP_001077354.2:n.*386G>A