Canonical Allele Identifier: CA2067685982
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997574C= , CM000674.2:g.120997574C= GRCh38
NC_000012.11:g.121435377C= , CM000674.1:g.121435377C= GRCh37
NC_000012.10:g.119919760C= NCBI36
NG_011731.2:g.23829C= , LRG_522:g.23829C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*157C= ENSP00000453965.2:n.*157C=
ENST00000257555.11:c.1410C= MANE Select ENSP00000257555.5:p.Pro470=
ENST00000257555.10:c.1410C= ENSP00000257555.4:p.Pro470=
ENST00000400024.6:c.1410C= ENSP00000476181.1:p.Pro470=
ENST00000402929.5:n.2276C=
ENST00000535955.5:n.126C=
ENST00000538626.2:n.274C=
ENST00000538646.5:c.*386C= ENSP00000443964.1:n.*386C=
ENST00000540108.1:c.*850C= ENSP00000445445.1:n.*850C=
ENST00000541395.5:c.1410C= ENSP00000443112.1:p.Pro470=
ENST00000541924.5:c.*424C= ENSP00000440361.1:n.*424C=
ENST00000543255.1:n.454C=
ENST00000543427.5:c.873C= ENSP00000439721.2:p.Pro291=
ENST00000544413.2:c.1410C= ENSP00000438804.1:p.Pro470=
ENST00000544574.5:c.*173C= ENSP00000438565.1:n.*173C=
ENST00000560968.5:c.1227C=
ENST00000615446.4:c.198C= ENSP00000483994.1:p.Pro66=
ENST00000617366.4:c.587-60C= ENSP00000481967.1:n.587-60C=
NM_000545.5:c.1410C= , LRG_522t1:c.1410C= NP_000536.5:p.Pro470=
NM_000545.6:c.1410C= NP_000536.5:p.Pro470=
NM_001306179.1:c.1410C= NP_001293108.1:p.Pro470=
XM_005253931.2:c.1410C= XP_005253988.1:p.Pro470=
XM_024449168.1:c.1410C= XP_024304936.1:p.Pro470=
NM_000545.8:c.1410C= MANE Select NP_000536.6:p.Pro470=
NM_001306179.2:c.1410C= NP_001293108.2:p.Pro470=