Canonical Allele Identifier: CA2695217533
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993704_120993712del , CM000674.2:g.120993704_120993712del GRCh38
NC_000012.11:g.121431507_121431515del , CM000674.1:g.121431507_121431515del GRCh37
NC_000012.10:g.119915890_119915898del NCBI36
NG_011731.2:g.19959_19967del , LRG_522:g.19959_19967del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.711_713+6del
ENST00000257555.11:c.711_713+6del
ENST00000257555.10:c.711_713+6del
ENST00000400024.6:c.711_713+6del
ENST00000402929.5:n.846_848+6del
ENST00000535955.5:n.43-3787_43-3779del
ENST00000538626.2:n.191-3787_191-3779del
ENST00000538646.5:c.527-460_527-452del ENSP00000443964.1:n.527-460_527-452del
ENST00000540108.1:c.*151_*153+6del
ENST00000541395.5:c.711_713+6del
ENST00000541924.5:c.711_713+6del
ENST00000543427.5:c.633+78_633+86del ENSP00000439721.2:n.633+78_633+86del
ENST00000544413.2:c.711_713+6del
ENST00000544574.5:c.73-2913_73-2905del ENSP00000438565.1:n.73-2913_73-2905del
ENST00000560968.5:c.854_856+6del
ENST00000615446.4:c.-257-2558_-257-2550del ENSP00000483994.1:n.-257-2558_-257-2550del
ENST00000617366.4:c.586+125_586+133del ENSP00000481967.1:n.586+125_586+133del
NM_000545.5:c.711_713+6del , LRG_522t1:c.711_713+6del
NM_000545.6:c.711_713+6del
NM_001306179.1:c.711_713+6del
XM_005253931.2:c.711_713+6del
XM_024449168.1:c.711_713+6del
NM_000545.8:c.711_713+6del
NM_001306179.2:c.711_713+6del