Canonical Allele Identifier: CA2573051300
Gene: HNF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1693220
ClinVar RCV Id: RCV002260480
dbSNP Id: rs2135832615

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120988905_120988911del , CM000674.2:g.120988905_120988911del GRCh38
NC_000012.11:g.121426708_121426714del , CM000674.1:g.121426708_121426714del GRCh37
NC_000012.10:g.119911091_119911097del NCBI36
NG_011731.2:g.15160_15166del , LRG_522:g.15160_15166del

Transcript Alleles

HGVS Amino-acid change
ENST00000560968.6:c.399_405del ENSP00000453965.2:p.Val134ProfsTer19
ENST00000257555.11:c.399_405del MANE Select ENSP00000257555.5:p.Val134ProfsTer19
ENST00000257555.10:c.399_405del ENSP00000257555.4:p.Val134ProfsTer19
ENST00000400024.6:c.399_405del ENSP00000476181.1:p.Val134ProfsTer19
ENST00000402929.5:n.534_540del
ENST00000535955.5:n.43-8586_43-8580del
ENST00000538626.2:n.191-8586_191-8580del
ENST00000538646.5:c.399_405del ENSP00000443964.1:p.Val134ProfsTer19
ENST00000540108.1:c.327-4615_327-4609del ENSP00000445445.1:n.327-4615_327-4609del
ENST00000541395.5:c.399_405del ENSP00000443112.1:p.Val134ProfsTer19
ENST00000541924.5:c.399_405del ENSP00000440361.1:p.Val134ProfsTer19
ENST00000543427.5:c.399_405del ENSP00000439721.2:p.Val134ProfsTer19
ENST00000544413.2:c.399_405del ENSP00000438804.1:p.Val134ProfsTer19
ENST00000544574.5:c.73-7712_73-7706del ENSP00000438565.1:n.73-7712_73-7706del
ENST00000560968.5:c.542_548del
ENST00000615446.4:c.-257-7357_-257-7351del ENSP00000483994.1:n.-257-7357_-257-7351de...
ENST00000617366.4:c.399_405del ENSP00000481967.1:p.Val134ProfsTer19
NM_000545.5:c.399_405del , LRG_522t1:c.399_405del NP_000536.5:p.Val134ProfsTer19
NM_000545.6:c.399_405del NP_000536.5:p.Val134ProfsTer19
NM_001306179.1:c.399_405del NP_001293108.1:p.Val134ProfsTer19
XM_005253931.2:c.399_405del XP_005253988.1:p.Val134ProfsTer19
XM_024449168.1:c.399_405del XP_024304936.1:p.Val134ProfsTer19
NM_000545.8:c.399_405del MANE Select NP_000536.6:p.Val134ProfsTer19
NM_001306179.2:c.399_405del NP_001293108.2:p.Val134ProfsTer19