Canonical Allele Identifier: CA2067680064
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994518A= , CM000674.2:g.120994518A= GRCh38
NC_000012.11:g.121432321A= , CM000674.1:g.121432321A= GRCh37
NC_000012.10:g.119916704A= NCBI36
NG_011731.2:g.20773A= , LRG_522:g.20773A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+318A= ENSP00000453965.2:n.750+318A=
ENST00000257555.11:c.955+113A= MANE Select ENSP00000257555.5:n.955+113A=
ENST00000257555.10:c.955+113A= ENSP00000257555.4:n.955+113A=
ENST00000400024.6:c.955+113A= ENSP00000476181.1:n.955+113A=
ENST00000402929.5:n.1090+113A=
ENST00000535955.5:n.43-2973A=
ENST00000538626.2:n.191-2973A=
ENST00000538646.5:c.768+113A= ENSP00000443964.1:n.768+113A=
ENST00000540108.1:c.*395+113A= ENSP00000445445.1:n.*395+113A=
ENST00000541395.5:c.955+113A= ENSP00000443112.1:n.955+113A=
ENST00000541924.5:c.713+812A= ENSP00000440361.1:n.713+812A=
ENST00000543427.5:c.633+892A= ENSP00000439721.2:n.633+892A=
ENST00000544413.2:c.955+113A= ENSP00000438804.1:n.955+113A=
ENST00000544574.5:c.73-2099A= ENSP00000438565.1:n.73-2099A=
ENST00000560968.5:c.893+318A=
ENST00000615446.4:c.-257-1744A= ENSP00000483994.1:n.-257-1744A=
ENST00000617366.4:c.586+939A= ENSP00000481967.1:n.586+939A=
NM_000545.5:c.955+113A= , LRG_522t1:c.955+113A= NP_000536.5:n.955+113A=
NM_000545.6:c.955+113A= NP_000536.5:n.955+113A=
NM_001306179.1:c.955+113A= NP_001293108.1:n.955+113A=
XM_005253931.2:c.955+113A= XP_005253988.1:n.955+113A=
XM_024449168.1:c.955+113A= XP_024304936.1:n.955+113A=
NM_000545.8:c.955+113A= MANE Select NP_000536.6:n.955+113A=
NM_001306179.2:c.955+113A= NP_001293108.2:n.955+113A=