Canonical Allele Identifier: CA2785655950
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114404133_114404134insACAT , CM000671.2:g.114404133_114404134insACAT GRCh38
NC_000009.11:g.117166413_117166414insACAT , CM000671.1:g.117166413_117166414insACAT GRCh37
NC_000009.10:g.116206234_116206235insACAT NCBI36
NG_016700.1:g.106323_106324insATGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000699485.1:c.581-57_581-56insATGT ENSP00000514396.1:n.581-57_581-56insATGT
ENST00000362057.4:c.2237-57_2237-56insATGT MANE Select ENSP00000354623.3:n.2237-57_2237-56insATGT
ENST00000674036.8:c.1210-57_1210-56insATGT
ENST00000674048.1:n.2118-57_2118-56insATGT
ENST00000265134.10:c.1088-57_1088-56insATGT ENSP00000265134.6:n.1088-57_1088-56insATGT
ENST00000362057.3:c.2237-57_2237-56insATGT ENSP00000354623.3:n.2237-57_2237-56insATGT
ENST00000374059.7:c.1184-57_1184-56insATGT ENSP00000363172.3:n.1184-57_1184-56insATGT
NM_001083885.2:c.1088-57_1088-56insATGT NP_001077354.2:n.1088-57_1088-56insATGT
NM_001173425.1:c.2237-60_2237-59insATGT NP_001166896.1:n.2237-60_2237-59insATGT
NM_015404.3:c.2237-57_2237-56insATGT NP_056219.3:n.2237-57_2237-56insATGT
XM_005251897.3:c.1574-57_1574-56insATGT XP_005251954.2:n.1574-57_1574-56insATGT
XM_011518484.1:c.2270-57_2270-56insATGT XP_011516786.1:n.2270-57_2270-56insATGT
XM_011518485.1:c.2270-57_2270-56insATGT XP_011516787.1:n.2270-57_2270-56insATGT
XM_011518486.1:c.2270-60_2270-59insATGT XP_011516788.1:n.2270-60_2270-59insATGT
XM_011518487.1:c.2144-57_2144-56insATGT XP_011516789.1:n.2144-57_2144-56insATGT
XM_011518488.1:c.2027-57_2027-56insATGT XP_011516790.1:n.2027-57_2027-56insATGT
XM_011518495.1:c.947-57_947-56insATGT XP_011516797.1:n.947-57_947-56insATGT
XR_929747.1:n.3174-57_3174-56insATGT
XR_929748.1:n.3072-57_3072-56insATGT
NM_001346890.1:c.1184-57_1184-56insATGT NP_001333819.1:n.1184-57_1184-56insATGT
XM_011518486.2:c.2270-60_2270-59insATGT XP_011516788.1:n.2270-60_2270-59insATGT
XM_011518487.2:c.2144-57_2144-56insATGT XP_011516789.1:n.2144-57_2144-56insATGT
XM_011518488.2:c.2027-57_2027-56insATGT XP_011516790.1:n.2027-57_2027-56insATGT
XR_929747.2:n.2485-57_2485-56insATGT
XR_929748.2:n.2383-57_2383-56insATGT
NM_015404.4:c.2237-57_2237-56insATGT MANE Select NP_056219.3:n.2237-57_2237-56insATGT
NM_001173425.2:c.2237-60_2237-59insATGT NP_001166896.1:n.2237-60_2237-59insATGT
NM_001083885.3:c.1088-57_1088-56insATGT NP_001077354.2:n.1088-57_1088-56insATGT