Canonical Allele Identifier: CA2067686332
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997670G= , CM000674.2:g.120997670G= GRCh38
NC_000012.11:g.121435473G= , CM000674.1:g.121435473G= GRCh37
NC_000012.10:g.119919856G= NCBI36
NG_011731.2:g.23925G= , LRG_522:g.23925G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+5G= ENSP00000453965.2:n.*248+5G=
ENST00000257555.11:c.1501+5G= MANE Select ENSP00000257555.5:n.1501+5G=
ENST00000257555.10:c.1501+5G= ENSP00000257555.4:n.1501+5G=
ENST00000400024.6:c.1506G= ENSP00000476181.1:p.Glu502=
ENST00000402929.5:n.2372G=
ENST00000535955.5:n.222G=
ENST00000538626.2:n.370G=
ENST00000538646.5:c.*482G= ENSP00000443964.1:n.*482G=
ENST00000540108.1:c.*941+5G= ENSP00000445445.1:n.*941+5G=
ENST00000541395.5:c.1501+5G= ENSP00000443112.1:n.1501+5G=
ENST00000541924.5:c.*520G= ENSP00000440361.1:n.*520G=
ENST00000543255.1:n.550G=
ENST00000543427.5:c.964+5G= ENSP00000439721.2:n.964+5G=
ENST00000544413.2:c.1501+5G= ENSP00000438804.1:n.1501+5G=
ENST00000544574.5:c.*269G= ENSP00000438565.1:n.*269G=
ENST00000560968.5:c.1318+5G=
ENST00000615446.4:c.289+5G= ENSP00000483994.1:n.289+5G=
ENST00000617366.4:c.618+5G= ENSP00000481967.1:n.618+5G=
NM_000545.5:c.1501+5G= , LRG_522t1:c.1501+5G= NP_000536.5:n.1501+5G=
NM_000545.6:c.1501+5G= NP_000536.5:n.1501+5G=
NM_001306179.1:c.1501+5G= NP_001293108.1:n.1501+5G=
XM_005253931.2:c.1501+5G= XP_005253988.1:n.1501+5G=
XM_024449168.1:c.1501+5G= XP_024304936.1:n.1501+5G=
NM_000545.8:c.1501+5G= MANE Select NP_000536.6:n.1501+5G=
NM_001306179.2:c.1501+5G= NP_001293108.2:n.1501+5G=