Canonical Allele Identifier: CA2067677897
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993342_120993343delinsTG , CM000674.2:g.120993342_120993343delinsTG GRCh38
NC_000012.11:g.121431145_121431146delinsTG , CM000674.1:g.121431145_121431146delinsTG GRCh37
NC_000012.10:g.119915528_119915529delinsTG NCBI36
NG_011731.2:g.19597_19598delinsTG , LRG_522:g.19597_19598delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.527-178_527-177delinsTG ENSP00000453965.2:n.527-178_527-177delinsTG
ENST00000257555.11:c.527-178_527-177delinsTG MANE Select ENSP00000257555.5:n.527-178_527-177delinsTG
ENST00000257555.10:c.527-178_527-177delinsTG ENSP00000257555.4:n.527-178_527-177delinsTG
ENST00000400024.6:c.527-178_527-177delinsTG ENSP00000476181.1:n.527-178_527-177delinsTG
ENST00000402929.5:n.662-178_662-177delinsTG
ENST00000535955.5:n.43-4149_43-4148delinsTG
ENST00000538626.2:n.191-4149_191-4148delinsTG
ENST00000538646.5:c.527-822_527-821delinsTG ENSP00000443964.1:n.527-822_527-821delinsTG
ENST00000540108.1:c.327-178_327-177delinsTG ENSP00000445445.1:n.327-178_327-177delinsTG
ENST00000541395.5:c.527-178_527-177delinsTG ENSP00000443112.1:n.527-178_527-177delinsTG
ENST00000541924.5:c.527-178_527-177delinsTG ENSP00000440361.1:n.527-178_527-177delinsTG
ENST00000543427.5:c.527-178_527-177delinsTG ENSP00000439721.2:n.527-178_527-177delinsTG
ENST00000544413.2:c.527-178_527-177delinsTG ENSP00000438804.1:n.527-178_527-177delinsTG
ENST00000544574.5:c.73-3275_73-3274delinsTG ENSP00000438565.1:n.73-3275_73-3274delinsTG
ENST00000560968.5:c.670-178_670-177delinsTG
ENST00000615446.4:c.-257-2920_-257-2919delinsTG ENSP00000483994.1:n.-257-2920_-257-2919delinsTG
ENST00000617366.4:c.527-178_527-177delinsTG ENSP00000481967.1:n.527-178_527-177delinsTG
NM_000545.5:c.527-178_527-177delinsTG , LRG_522t1:c.527-178_527-177delinsTG NP_000536.5:n.527-178_527-177delinsTG
NM_000545.6:c.527-178_527-177delinsTG NP_000536.5:n.527-178_527-177delinsTG
NM_001306179.1:c.527-178_527-177delinsTG NP_001293108.1:n.527-178_527-177delinsTG
XM_005253931.2:c.527-178_527-177delinsTG XP_005253988.1:n.527-178_527-177delinsTG
XM_024449168.1:c.527-178_527-177delinsTG XP_024304936.1:n.527-178_527-177delinsTG
NM_000545.8:c.527-178_527-177delinsTG MANE Select NP_000536.6:n.527-178_527-177delinsTG
NM_001306179.2:c.527-178_527-177delinsTG NP_001293108.2:n.527-178_527-177delinsTG