Canonical Allele Identifier: CA2067686471
Gene: HNF1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997709T= , CM000674.2:g.120997709T= GRCh38
NC_000012.11:g.121435512T= , CM000674.1:g.121435512T= GRCh37
NC_000012.10:g.119919895T= NCBI36
NG_011731.2:g.23964T= , LRG_522:g.23964T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+44T= ENSP00000453965.2:n.*248+44T=
ENST00000257555.11:c.1501+44T= MANE Select ENSP00000257555.5:n.1501+44T=
ENST00000257555.10:c.1501+44T= ENSP00000257555.4:n.1501+44T=
ENST00000400024.6:c.1545T= ENSP00000476181.1:p.Gly515=
ENST00000402929.5:n.2411T=
ENST00000535955.5:n.261T=
ENST00000538626.2:n.409T=
ENST00000538646.5:c.*521T= ENSP00000443964.1:n.*521T=
ENST00000540108.1:c.*941+44T= ENSP00000445445.1:n.*941+44T=
ENST00000541395.5:c.1501+44T= ENSP00000443112.1:n.1501+44T=
ENST00000541924.5:c.*559T= ENSP00000440361.1:n.*559T=
ENST00000543255.1:n.589T=
ENST00000543427.5:c.964+44T= ENSP00000439721.2:n.964+44T=
ENST00000544413.2:c.1501+44T= ENSP00000438804.1:n.1501+44T=
ENST00000544574.5:c.*308T= ENSP00000438565.1:n.*308T=
ENST00000560968.5:c.1318+44T=
ENST00000615446.4:c.289+44T= ENSP00000483994.1:n.289+44T=
ENST00000617366.4:c.618+44T= ENSP00000481967.1:n.618+44T=
NM_000545.5:c.1501+44T= , LRG_522t1:c.1501+44T= NP_000536.5:n.1501+44T=
NM_000545.6:c.1501+44T= NP_000536.5:n.1501+44T=
NM_001306179.1:c.1501+44T= NP_001293108.1:n.1501+44T=
XM_005253931.2:c.1501+44T= XP_005253988.1:n.1501+44T=
XM_024449168.1:c.1501+44T= XP_024304936.1:n.1501+44T=
NM_000545.8:c.1501+44T= MANE Select NP_000536.6:n.1501+44T=
NM_001306179.2:c.1501+44T= NP_001293108.2:n.1501+44T=
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