Canonical Allele Identifier: CA858984536

Gene: WHRN

Linked Data

• dbSNP Id: rs1305548225
• gnomAD v3: 9-114402578-T-C
• gnomAD v4: 9-114402578-T-C
• MyVariant Identifiers: chr9:g.117164858T>C (hg19) ; chr9:g.114402578T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402578T>C , CM000671.2:g.114402578T>C	GRCh38
NC_000009.11:g.117164858T>C , CM000671.1:g.117164858T>C	GRCh37
NC_000009.10:g.116204679T>C	NCBI36
NG_016700.1:g.107879A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.1244A>G	ENSP00000514396.1:n.1244A>G
ENST00000362057.4:c.*176A>G MANE Select	ENSP00000354623.3:n.*176A>G
ENST00000674036.8:c.1873A>G
ENST00000674048.1:n.2781A>G
ENST00000265134.10:c.*176A>G	ENSP00000265134.6:n.*176A>G
ENST00000362057.3:c.*176A>G	ENSP00000354623.3:n.*176A>G
ENST00000374059.7:c.*176A>G	ENSP00000363172.3:n.*176A>G
NM_001083885.2:c.*176A>G	NP_001077354.2:n.*176A>G
NM_001173425.1:c.*176A>G	NP_001166896.1:n.*176A>G
NM_015404.3:c.*176A>G	NP_056219.3:n.*176A>G
XM_005251897.3:c.*176A>G	XP_005251954.2:n.*176A>G
XM_011518484.1:c.*176A>G	XP_011516786.1:n.*176A>G
XM_011518485.1:c.*176A>G	XP_011516787.1:n.*176A>G
XM_011518486.1:c.*176A>G	XP_011516788.1:n.*176A>G
XM_011518487.1:c.*176A>G	XP_011516789.1:n.*176A>G
XM_011518488.1:c.*176A>G	XP_011516790.1:n.*176A>G
XM_011518495.1:c.*176A>G	XP_011516797.1:n.*176A>G
NM_001346890.1:c.*176A>G	NP_001333819.1:n.*176A>G
XM_011518486.2:c.*176A>G	XP_011516788.1:n.*176A>G
XM_011518487.2:c.*176A>G	XP_011516789.1:n.*176A>G
XM_011518488.2:c.*176A>G	XP_011516790.1:n.*176A>G
NM_015404.4:c.*176A>G MANE Select	NP_056219.3:n.*176A>G
NM_001173425.2:c.*176A>G	NP_001166896.1:n.*176A>G
NM_001083885.3:c.*176A>G	NP_001077354.2:n.*176A>G