Canonical Allele Identifier: CA2067685969
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997572_120997575delinsCCCT , CM000674.2:g.120997572_120997575delinsCCCT GRCh38
NC_000012.11:g.121435375_121435378delinsCCCT , CM000674.1:g.121435375_121435378delinsCCCT GRCh37
NC_000012.10:g.119919758_119919761delinsCCCT NCBI36
NG_011731.2:g.23827_23830delinsCCCT , LRG_522:g.23827_23830delinsCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*155_*158delinsCCCT ENSP00000453965.2:n.*155_*158delinsCCCT
ENST00000257555.11:c.1408_1411delinsCCCT MANE Select ENSP00000257555.5:p.Pro470=
ENST00000257555.10:c.1408_1411delinsCCCT ENSP00000257555.4:p.Pro470=
ENST00000400024.6:c.1408_1411delinsCCCT ENSP00000476181.1:p.Pro470=
ENST00000402929.5:n.2274_2277delinsCCCT
ENST00000535955.5:n.124_127delinsCCCT
ENST00000538626.2:n.272_275delinsCCCT
ENST00000538646.5:c.*384_*387delinsCCCT ENSP00000443964.1:n.*384_*387delinsCCCT
ENST00000540108.1:c.*848_*851delinsCCCT ENSP00000445445.1:n.*848_*851delinsCCCT
ENST00000541395.5:c.1408_1411delinsCCCT ENSP00000443112.1:p.Pro470=
ENST00000541924.5:c.*422_*425delinsCCCT ENSP00000440361.1:n.*422_*425delinsCCCT
ENST00000543255.1:n.452_455delinsCCCT
ENST00000543427.5:c.871_874delinsCCCT ENSP00000439721.2:p.Pro291=
ENST00000544413.2:c.1408_1411delinsCCCT ENSP00000438804.1:p.Pro470=
ENST00000544574.5:c.*171_*174delinsCCCT ENSP00000438565.1:n.*171_*174delinsCCCT
ENST00000560968.5:c.1225_1228delinsCCCT
ENST00000615446.4:c.196_199delinsCCCT ENSP00000483994.1:p.Pro66=
ENST00000617366.4:c.587-62_587-59delinsCCCT ENSP00000481967.1:n.587-62_587-59delinsCCCT
NM_000545.5:c.1408_1411delinsCCCT , LRG_522t1:c.1408_1411delinsCCCT NP_000536.5:p.Pro470=
NM_000545.6:c.1408_1411delinsCCCT NP_000536.5:p.Pro470=
NM_001306179.1:c.1408_1411delinsCCCT NP_001293108.1:p.Pro470=
XM_005253931.2:c.1408_1411delinsCCCT XP_005253988.1:p.Pro470=
XM_024449168.1:c.1408_1411delinsCCCT XP_024304936.1:p.Pro470=
NM_000545.8:c.1408_1411delinsCCCT MANE Select NP_000536.6:p.Pro470=
NM_001306179.2:c.1408_1411delinsCCCT NP_001293108.2:p.Pro470=