Canonical Allele Identifier: CA2067680091
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994570_120994574delinsCTCTA , CM000674.2:g.120994570_120994574delinsCTCTA GRCh38
NC_000012.11:g.121432373_121432377delinsCTCTA , CM000674.1:g.121432373_121432377delinsCTCTA GRCh37
NC_000012.10:g.119916756_119916760delinsCTCTA NCBI36
NG_011731.2:g.20825_20829delinsCTCTA , LRG_522:g.20825_20829delinsCTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+370_750+374delinsCTCTA ENSP00000453965.2:n.750+370_750+374delinsCTCTA
ENST00000257555.11:c.955+165_955+169delinsCTCTA MANE Select ENSP00000257555.5:n.955+165_955+169delinsCTCTA
ENST00000257555.10:c.955+165_955+169delinsCTCTA ENSP00000257555.4:n.955+165_955+169delinsCTCTA
ENST00000400024.6:c.955+165_955+169delinsCTCTA ENSP00000476181.1:n.955+165_955+169delinsCTCTA
ENST00000402929.5:n.1090+165_1090+169delinsCTCTA
ENST00000535955.5:n.43-2921_43-2917delinsCTCTA
ENST00000538626.2:n.191-2921_191-2917delinsCTCTA
ENST00000538646.5:c.768+165_768+169delinsCTCTA ENSP00000443964.1:n.768+165_768+169delinsCTCTA
ENST00000540108.1:c.*395+165_*395+169delinsCTCTA ENSP00000445445.1:n.*395+165_*395+169delinsCTCTA
ENST00000541395.5:c.955+165_955+169delinsCTCTA ENSP00000443112.1:n.955+165_955+169delinsCTCTA
ENST00000541924.5:c.713+864_713+868delinsCTCTA ENSP00000440361.1:n.713+864_713+868delinsCTCTA
ENST00000543427.5:c.633+944_633+948delinsCTCTA ENSP00000439721.2:n.633+944_633+948delinsCTCTA
ENST00000544413.2:c.955+165_955+169delinsCTCTA ENSP00000438804.1:n.955+165_955+169delinsCTCTA
ENST00000544574.5:c.73-2047_73-2043delinsCTCTA ENSP00000438565.1:n.73-2047_73-2043delinsCTCTA
ENST00000560968.5:c.893+370_893+374delinsCTCTA
ENST00000615446.4:c.-257-1692_-257-1688delinsCTCTA ENSP00000483994.1:n.-257-1692_-257-1688delinsCTCTA
ENST00000617366.4:c.586+991_586+995delinsCTCTA ENSP00000481967.1:n.586+991_586+995delinsCTCTA
NM_000545.5:c.955+165_955+169delinsCTCTA , LRG_522t1:c.955+165_955+169delinsCTCTA NP_000536.5:n.955+165_955+169delinsCTCTA
NM_000545.6:c.955+165_955+169delinsCTCTA NP_000536.5:n.955+165_955+169delinsCTCTA
NM_001306179.1:c.955+165_955+169delinsCTCTA NP_001293108.1:n.955+165_955+169delinsCTCTA
XM_005253931.2:c.955+165_955+169delinsCTCTA XP_005253988.1:n.955+165_955+169delinsCTCTA
XM_024449168.1:c.955+165_955+169delinsCTCTA XP_024304936.1:n.955+165_955+169delinsCTCTA
NM_000545.8:c.955+165_955+169delinsCTCTA MANE Select NP_000536.6:n.955+165_955+169delinsCTCTA
NM_001306179.2:c.955+165_955+169delinsCTCTA NP_001293108.2:n.955+165_955+169delinsCTCTA