Canonical Allele Identifier: CA244535856
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs151344539

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120999090dup , CM000674.2:g.120999090dup GRCh38
NC_000012.11:g.121436893dup , CM000674.1:g.121436893dup GRCh37
NC_000012.10:g.119921276dup NCBI36
NG_011731.2:g.25345dup , LRG_522:g.25345dup

Transcript Alleles

HGVS Amino-acid change
ENST00000560968.6:c.*249-178dup ENSP00000453965.2:n.*249-178dup
ENST00000257555.11:c.1502-178dup MANE Select ENSP00000257555.5:n.1502-178dup
ENST00000257555.10:c.1502-178dup ENSP00000257555.4:n.1502-178dup
ENST00000540108.1:c.*942-178dup ENSP00000445445.1:n.*942-178dup
ENST00000541395.5:c.1502-178dup ENSP00000443112.1:n.1502-178dup
ENST00000543427.5:c.965-178dup ENSP00000439721.2:n.965-178dup
ENST00000544413.2:c.1502-178dup ENSP00000438804.1:n.1502-178dup
ENST00000560968.5:c.1319-178dup
ENST00000615446.4:c.290-178dup ENSP00000483994.1:n.290-178dup
ENST00000617366.4:c.619-178dup ENSP00000481967.1:n.619-178dup
NM_000545.5:c.1502-178dup , LRG_522t1:c.1502-178dup NP_000536.5:n.1502-178dup
NM_000545.6:c.1502-178dup NP_000536.5:n.1502-178dup
NM_001306179.1:c.1502-178dup NP_001293108.1:n.1502-178dup
XM_005253931.2:c.1502-178dup XP_005253988.1:n.1502-178dup
XM_024449168.1:c.1502-178dup XP_024304936.1:n.1502-178dup
NM_000545.8:c.1502-178dup MANE Select NP_000536.6:n.1502-178dup
NM_001306179.2:c.1502-178dup NP_001293108.2:n.1502-178dup