Canonical Allele Identifier: CA1873827845
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114407968G= , CM000671.2:g.114407968G= GRCh38
NC_000009.11:g.117170248G= , CM000671.1:g.117170248G= GRCh37
NC_000009.10:g.116210069G= NCBI36
NG_016700.1:g.102489C=

Transcript Alleles

HGVS Amino-acid change
ENST00000362057.4:c.1677C= MANE Select ENSP00000354623.3:p.Asn559=
ENST00000673811.1:n.2401C=
ENST00000674036.8:c.650C=
ENST00000674048.1:n.1558C=
ENST00000265134.10:c.528C= ENSP00000265134.6:p.Asn176=
ENST00000362057.3:c.1677C= ENSP00000354623.3:p.Asn559=
ENST00000374059.7:c.624C= ENSP00000363172.3:p.Asn208=
NM_001083885.2:c.528C= NP_001077354.2:p.Asn176=
NM_001173425.1:c.1677C= NP_001166896.1:p.Asn559=
NM_015404.3:c.1677C= NP_056219.3:p.Asn559=
XM_005251897.3:c.1014C= XP_005251954.2:p.Asn338=
XM_011518484.1:c.1710C= XP_011516786.1:p.Asn570=
XM_011518485.1:c.1710C= XP_011516787.1:p.Asn570=
XM_011518486.1:c.1710C= XP_011516788.1:p.Asn570=
XM_011518487.1:c.1584C= XP_011516789.1:p.Asn528=
XM_011518488.1:c.1467C= XP_011516790.1:p.Asn489=
XM_011518492.1:c.*62C= XP_011516794.1:n.*62C=
XM_011518495.1:c.387C= XP_011516797.1:p.Asn129=
XR_929747.1:n.2614C=
XR_929748.1:n.2512C=
XR_929750.1:n.2613C=
XR_929751.1:n.2520C=
XR_929757.1:n.2487C=
NM_001346890.1:c.624C= NP_001333819.1:p.Asn208=
XM_011518486.2:c.1710C= XP_011516788.1:p.Asn570=
XM_011518487.2:c.1584C= XP_011516789.1:p.Asn528=
XM_011518488.2:c.1467C= XP_011516790.1:p.Asn489=
XM_011518492.2:c.*62C= XP_011516794.1:n.*62C=
XR_929747.2:n.1925C=
XR_929748.2:n.1823C=
XR_929750.3:n.1924C=
XR_929757.2:n.1798C=
NM_015404.4:c.1677C= MANE Select NP_056219.3:p.Asn559=
NM_001173425.2:c.1677C= NP_001166896.1:p.Asn559=
NM_001083885.3:c.528C= NP_001077354.2:p.Asn176=