Canonical Allele Identifier: CA374609091
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1026499
ClinVar RCV Id: RCV001326958
dbSNP Id: rs1836631124

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114424512A>T , CM000671.2:g.114424512A>T GRCh38
NC_000009.11:g.117186792A>T , CM000671.1:g.117186792A>T GRCh37
NC_000009.10:g.116226613A>T NCBI36
NG_016700.1:g.85945T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699486.1:c.962T>A ENSP00000514397.1:p.Val321Glu
ENST00000362057.4:c.1238T>A MANE Select ENSP00000354623.3:p.Val413Glu
ENST00000673811.1:n.2172T>A
ENST00000674036.8:c.421T>A
ENST00000674048.1:n.1119T>A
ENST00000265134.10:c.89T>A ENSP00000265134.6:p.Val30Glu
ENST00000362057.3:c.1238T>A ENSP00000354623.3:p.Val413Glu
ENST00000374059.7:c.185T>A ENSP00000363172.3:p.Val62Glu
NM_001083885.2:c.89T>A NP_001077354.2:p.Val30Glu
NM_001173425.1:c.1238T>A NP_001166896.1:p.Val413Glu
NM_015404.3:c.1238T>A NP_056219.3:p.Val413Glu
XM_005251897.3:c.964-16494T>A XP_005251954.2:n.964-16494T>A
XM_011518484.1:c.1238T>A XP_011516786.1:p.Val413Glu
XM_011518485.1:c.1238T>A XP_011516787.1:p.Val413Glu
XM_011518486.1:c.1238T>A XP_011516788.1:p.Val413Glu
XM_011518487.1:c.1112T>A XP_011516789.1:p.Val371Glu
XM_011518488.1:c.1238T>A XP_011516790.1:p.Val413Glu
XM_011518489.1:c.1238T>A XP_011516791.1:p.Val413Glu
XM_011518490.1:c.1238T>A XP_011516792.1:p.Val413Glu
XM_011518491.1:c.1238T>A XP_011516793.1:p.Val413Glu
XM_011518492.1:c.1238T>A XP_011516794.1:p.Val413Glu
XM_011518493.1:c.1238T>A XP_011516795.1:p.Val413Glu
XM_011518494.1:c.1238T>A XP_011516796.1:p.Val413Glu
XM_011518495.1:c.-86T>A XP_011516797.1:n.-86T>A
XR_929747.1:n.1946T>A
XR_929748.1:n.1946T>A
XR_929749.1:n.1946T>A
XR_929750.1:n.1946T>A
XR_929751.1:n.1946T>A
XR_929752.1:n.1946T>A
XR_929753.1:n.1946T>A
XR_929754.1:n.1946T>A
XR_929755.1:n.1946T>A
XR_929756.1:n.1946T>A
XR_929757.1:n.1946T>A
NM_001346890.1:c.185T>A NP_001333819.1:p.Val62Glu
XM_011518486.2:c.1238T>A XP_011516788.1:p.Val413Glu
XM_011518487.2:c.1112T>A XP_011516789.1:p.Val371Glu
XM_011518488.2:c.1238T>A XP_011516790.1:p.Val413Glu
XM_011518489.3:c.1238T>A XP_011516791.1:p.Val413Glu
XM_011518491.3:c.1238T>A XP_011516793.1:p.Val413Glu
XM_011518492.2:c.1238T>A XP_011516794.1:p.Val413Glu
XM_011518494.3:c.1238T>A XP_011516796.1:p.Val413Glu
XR_929747.2:n.1257T>A
XR_929748.2:n.1257T>A
XR_929749.2:n.1257T>A
XR_929750.3:n.1257T>A
XR_929752.2:n.1257T>A
XR_929753.3:n.1257T>A
XR_929754.2:n.1257T>A
XR_929755.3:n.1257T>A
XR_929756.2:n.1257T>A
XR_929757.2:n.1257T>A
NM_015404.4:c.1238T>A MANE Select NP_056219.3:p.Val413Glu
NM_001173425.2:c.1238T>A NP_001166896.1:p.Val413Glu
NM_001083885.3:c.89T>A NP_001077354.2:p.Val30Glu