Canonical Allele Identifier: CA2573051034
Gene: HNF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1676685
ClinVar RCV Id: RCV002222082
dbSNP Id: rs2135819834

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120978932_120978936del , CM000674.2:g.120978932_120978936del GRCh38
NC_000012.11:g.121416735_121416739del , CM000674.1:g.121416735_121416739del GRCh37
NC_000012.10:g.119901118_119901122del NCBI36
NG_011731.2:g.5187_5191del , LRG_522:g.5187_5191del

Transcript Alleles

HGVS Amino-acid change
ENST00000560968.6:c.164_168del ENSP00000453965.2:p.Gly55AlafsTer3
ENST00000257555.11:c.164_168del MANE Select ENSP00000257555.5:p.Gly55AlafsTer3
ENST00000257555.10:c.164_168del ENSP00000257555.4:p.Gly55AlafsTer3
ENST00000400024.6:c.164_168del ENSP00000476181.1:p.Gly55AlafsTer3
ENST00000402929.5:n.299_303del
ENST00000535955.5:n.42+240_42+244del
ENST00000538626.2:n.190+92_190+96del
ENST00000538646.5:c.164_168del ENSP00000443964.1:p.Gly55AlafsTer3
ENST00000540108.1:c.164_168del ENSP00000445445.1:p.Gly55AlafsTer3
ENST00000541395.5:c.164_168del ENSP00000443112.1:p.Gly55AlafsTer3
ENST00000541924.5:c.164_168del ENSP00000440361.1:p.Gly55AlafsTer3
ENST00000543427.5:c.164_168del ENSP00000439721.2:p.Gly55AlafsTer3
ENST00000544413.2:c.164_168del ENSP00000438804.1:p.Gly55AlafsTer3
ENST00000544574.5:c.72+92_72+96del ENSP00000438565.1:n.72+92_72+96del
ENST00000560968.5:c.307_311del
ENST00000615446.4:c.-258+221_-258+225del ENSP00000483994.1:n.-258+221_-258+225del
ENST00000617366.4:c.164_168del ENSP00000481967.1:p.Gly55AlafsTer3
NM_000545.5:c.164_168del , LRG_522t1:c.164_168del NP_000536.5:p.Gly55AlafsTer3
NM_000545.6:c.164_168del NP_000536.5:p.Gly55AlafsTer3
NM_001306179.1:c.164_168del NP_001293108.1:p.Gly55AlafsTer3
XM_005253931.2:c.164_168del XP_005253988.1:p.Gly55AlafsTer3
XM_024449168.1:c.164_168del XP_024304936.1:p.Gly55AlafsTer3
NM_000545.8:c.164_168del MANE Select NP_000536.6:p.Gly55AlafsTer3
NM_001306179.2:c.164_168del NP_001293108.2:p.Gly55AlafsTer3