Canonical Allele Identifier: CA658799362
Gene: HNF4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44406108del , CM000682.2:g.44406108del GRCh38
NC_000020.10:g.43034748del , CM000682.1:g.43034748del GRCh37
NC_000020.9:g.42468162del NCBI36
NG_009818.1:g.55308del , LRG_483:g.55308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.100del MANE Select ENSP00000315180.4:p.Val34SerfsTer?
ENST00000316099.10:c.166del ENSP00000312987.3:p.Val56SerfsTer?
ENST00000619550.5:c.140del
ENST00000681977.1:c.142del ENSP00000507189.1:p.Val48SerfsTer?
ENST00000682169.1:c.119del
ENST00000683148.1:n.142del
ENST00000683657.1:n.142del
ENST00000684046.1:c.142del ENSP00000507555.1:p.Val48SerfsTer?
ENST00000684136.1:c.142del ENSP00000507389.1:p.Val48SerfsTer?
ENST00000684476.1:c.123del ENSP00000507529.1:p.Ser42GlnfsTer22
ENST00000316099.9:c.166del ENSP00000312987.3:p.Val56SerfsTer?
ENST00000316099.8:c.166del ENSP00000312987.3:p.Val56SerfsTer?
ENST00000316673.8:c.100del ENSP00000315180.4:p.Val34SerfsTer?
ENST00000372920.1:c.257del ENSP00000362011.1:p.Cys86PhefsTer?
ENST00000415691.2:c.166del ENSP00000412111.1:p.Val56SerfsTer?
ENST00000443598.6:c.166del ENSP00000410911.2:p.Val56SerfsTer?
ENST00000457232.5:c.100del ENSP00000396216.1:p.Val34SerfsTer?
ENST00000609262.5:c.91del ENSP00000476310.1:p.Val31SerfsTer?
ENST00000609795.5:c.100del ENSP00000476609.1:p.Val34SerfsTer?
ENST00000619550.4:c.91del ENSP00000481331.1:p.Val31SerfsTer?
NM_000457.4:c.166del , LRG_483t2:c.166del NP_000448.3:p.Val56SerfsTer?
NM_001030003.2:c.100del NP_001025174.1:p.Val34SerfsTer?
NM_001030004.2:c.100del NP_001025175.1:p.Val34SerfsTer?
NM_001258355.1:c.145del NP_001245284.1:p.Val49SerfsTer?
NM_001287182.1:c.91del NP_001274111.1:p.Val31SerfsTer?
NM_001287183.1:c.91del , LRG_483t3:c.91del NP_001274112.1:p.Val31SerfsTer?
NM_001287184.1:c.91del NP_001274113.1:p.Val31SerfsTer?
NM_175914.4:c.100del , LRG_483t1:c.100del NP_787110.2:p.Val34SerfsTer?
NM_178849.2:c.166del NP_849180.1:p.Val56SerfsTer?
NM_178850.2:c.166del NP_849181.1:p.Val56SerfsTer?
XM_005260407.2:c.283del XP_005260464.1:p.Val95SerfsTer?
XM_011528797.1:c.214del XP_011527099.1:p.Val72SerfsTer?
XM_011528798.1:c.214del XP_011527100.1:p.Val72SerfsTer?
XM_005260407.4:c.283del XP_005260464.1:p.Val95SerfsTer?
NM_001030003.3:c.100del NP_001025174.1:p.Val34SerfsTer?
NM_001030004.3:c.100del NP_001025175.1:p.Val34SerfsTer?
NM_001258355.2:c.145del NP_001245284.1:p.Val49SerfsTer?
NM_001287182.2:c.91del NP_001274111.1:p.Val31SerfsTer?
NM_001287184.2:c.91del NP_001274113.1:p.Val31SerfsTer?
NM_178849.3:c.166del NP_849180.1:p.Val56SerfsTer?
NM_178850.3:c.166del NP_849181.1:p.Val56SerfsTer?
NM_000457.5:c.166del NP_000448.3:p.Val56SerfsTer?
NM_000457.6:c.166del NP_000448.3:p.Val56SerfsTer?
NM_001287183.2:c.91del NP_001274112.1:p.Val31SerfsTer?
NM_175914.5:c.100del MANE Select NP_787110.2:p.Val34SerfsTer?