Canonical Allele Identifier: CA2067672853
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120988996A= , CM000674.2:g.120988996A= GRCh38
NC_000012.11:g.121426799A= , CM000674.1:g.121426799A= GRCh37
NC_000012.10:g.119911182A= NCBI36
NG_011731.2:g.15251A= , LRG_522:g.15251A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.490A= ENSP00000453965.2:p.Thr164=
ENST00000257555.11:c.490A= MANE Select ENSP00000257555.5:p.Thr164=
ENST00000257555.10:c.490A= ENSP00000257555.4:p.Thr164=
ENST00000400024.6:c.490A= ENSP00000476181.1:p.Thr164=
ENST00000402929.5:n.625A=
ENST00000535955.5:n.43-8495A=
ENST00000538626.2:n.191-8495A=
ENST00000538646.5:c.490A= ENSP00000443964.1:p.Thr164=
ENST00000540108.1:c.327-4524A= ENSP00000445445.1:n.327-4524A=
ENST00000541395.5:c.490A= ENSP00000443112.1:p.Thr164=
ENST00000541924.5:c.490A= ENSP00000440361.1:p.Thr164=
ENST00000543427.5:c.490A= ENSP00000439721.2:p.Thr164=
ENST00000544413.2:c.490A= ENSP00000438804.1:p.Thr164=
ENST00000544574.5:c.73-7621A= ENSP00000438565.1:n.73-7621A=
ENST00000560968.5:c.633A=
ENST00000615446.4:c.-257-7266A= ENSP00000483994.1:n.-257-7266A=
ENST00000617366.4:c.490A= ENSP00000481967.1:p.Thr164=
NM_000545.5:c.490A= , LRG_522t1:c.490A= NP_000536.5:p.Thr164=
NM_000545.6:c.490A= NP_000536.5:p.Thr164=
NM_001306179.1:c.490A= NP_001293108.1:p.Thr164=
XM_005253931.2:c.490A= XP_005253988.1:p.Thr164=
XM_024449168.1:c.490A= XP_024304936.1:p.Thr164=
NM_000545.8:c.490A= MANE Select NP_000536.6:p.Thr164=
NM_001306179.2:c.490A= NP_001293108.2:p.Thr164=