Canonical Allele Identifier: CA2067686827
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997812C= , CM000674.2:g.120997812C= GRCh38
NC_000012.11:g.121435615C= , CM000674.1:g.121435615C= GRCh37
NC_000012.10:g.119919998C= NCBI36
NG_011731.2:g.24067C= , LRG_522:g.24067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+147C= ENSP00000453965.2:n.*248+147C=
ENST00000257555.11:c.1501+147C= MANE Select ENSP00000257555.5:n.1501+147C=
ENST00000257555.10:c.1501+147C= ENSP00000257555.4:n.1501+147C=
ENST00000400024.6:c.*19C= ENSP00000476181.1:n.*19C=
ENST00000402929.5:n.2514C=
ENST00000535955.5:n.364C=
ENST00000538626.2:n.512C=
ENST00000538646.5:c.*624C= ENSP00000443964.1:n.*624C=
ENST00000540108.1:c.*941+147C= ENSP00000445445.1:n.*941+147C=
ENST00000541395.5:c.1501+147C= ENSP00000443112.1:n.1501+147C=
ENST00000541924.5:c.*662C= ENSP00000440361.1:n.*662C=
ENST00000543255.1:n.692C=
ENST00000543427.5:c.964+147C= ENSP00000439721.2:n.964+147C=
ENST00000544413.2:c.1501+147C= ENSP00000438804.1:n.1501+147C=
ENST00000544574.5:c.*411C= ENSP00000438565.1:n.*411C=
ENST00000560968.5:c.1318+147C=
ENST00000615446.4:c.289+147C= ENSP00000483994.1:n.289+147C=
ENST00000617366.4:c.618+147C= ENSP00000481967.1:n.618+147C=
NM_000545.5:c.1501+147C= , LRG_522t1:c.1501+147C= NP_000536.5:n.1501+147C=
NM_000545.6:c.1501+147C= NP_000536.5:n.1501+147C=
NM_001306179.1:c.1501+147C= NP_001293108.1:n.1501+147C=
XM_005253931.2:c.1501+147C= XP_005253988.1:n.1501+147C=
XM_024449168.1:c.1501+147C= XP_024304936.1:n.1501+147C=
NM_000545.8:c.1501+147C= MANE Select NP_000536.6:n.1501+147C=
NM_001306179.2:c.1501+147C= NP_001293108.2:n.1501+147C=