Canonical Allele Identifier: CA386970332
Gene: HNF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997637C>A , CM000674.2:g.120997637C>A GRCh38
NC_000012.11:g.121435440C>A , CM000674.1:g.121435440C>A GRCh37
NC_000012.10:g.119919823C>A NCBI36
NG_011731.2:g.23892C>A , LRG_522:g.23892C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*220C>A ENSP00000453965.2:n.*220C>A
ENST00000257555.11:c.1473C>A MANE Select ENSP00000257555.5:p.Ala491=
ENST00000257555.10:c.1473C>A ENSP00000257555.4:p.Ala491=
ENST00000400024.6:c.1473C>A ENSP00000476181.1:p.Ala491=
ENST00000402929.5:n.2339C>A
ENST00000535955.5:n.189C>A
ENST00000538626.2:n.337C>A
ENST00000538646.5:c.*449C>A ENSP00000443964.1:n.*449C>A
ENST00000540108.1:c.*913C>A ENSP00000445445.1:n.*913C>A
ENST00000541395.5:c.1473C>A ENSP00000443112.1:p.Ala491=
ENST00000541924.5:c.*487C>A ENSP00000440361.1:n.*487C>A
ENST00000543255.1:n.517C>A
ENST00000543427.5:c.936C>A ENSP00000439721.2:p.Ala312=
ENST00000544413.2:c.1473C>A ENSP00000438804.1:p.Ala491=
ENST00000544574.5:c.*236C>A ENSP00000438565.1:n.*236C>A
ENST00000560968.5:c.1290C>A
ENST00000615446.4:c.261C>A ENSP00000483994.1:p.Ala87=
ENST00000617366.4:c.590C>A ENSP00000481967.1:p.Pro197Gln
NM_000545.5:c.1473C>A , LRG_522t1:c.1473C>A NP_000536.5:p.Ala491=
NM_000545.6:c.1473C>A NP_000536.5:p.Ala491=
NM_001306179.1:c.1473C>A NP_001293108.1:p.Ala491=
XM_005253931.2:c.1473C>A XP_005253988.1:p.Ala491=
XM_024449168.1:c.1473C>A XP_024304936.1:p.Ala491=
NM_000545.8:c.1473C>A MANE Select NP_000536.6:p.Ala491=
NM_001306179.2:c.1473C>A NP_001293108.2:p.Ala491=