Canonical Allele Identifier: CA684425117
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs1384798225

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997784_120997785del , CM000674.2:g.120997784_120997785del GRCh38
NC_000012.11:g.121435587_121435588del , CM000674.1:g.121435587_121435588del GRCh37
NC_000012.10:g.119919970_119919971del NCBI36
NG_011731.2:g.24039_24040del , LRG_522:g.24039_24040del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+119_*248+120del ENSP00000453965.2:n.*248+119_*248+120del
ENST00000257555.11:c.1501+119_1501+120del MANE Select ENSP00000257555.5:n.1501+119_1501+120del
ENST00000257555.10:c.1501+119_1501+120del ENSP00000257555.4:n.1501+119_1501+120del
ENST00000400024.6:c.1620_1621del ENSP00000476181.1:p.Phe541SerfsTer27
ENST00000402929.5:n.2486_2487del
ENST00000535955.5:n.336_337del
ENST00000538626.2:n.484_485del
ENST00000538646.5:c.*596_*597del ENSP00000443964.1:n.*596_*597del
ENST00000540108.1:c.*941+119_*941+120del ENSP00000445445.1:n.*941+119_*941+120del
ENST00000541395.5:c.1501+119_1501+120del ENSP00000443112.1:n.1501+119_1501+120del
ENST00000541924.5:c.*634_*635del ENSP00000440361.1:n.*634_*635del
ENST00000543255.1:n.664_665del
ENST00000543427.5:c.964+119_964+120del ENSP00000439721.2:n.964+119_964+120del
ENST00000544413.2:c.1501+119_1501+120del ENSP00000438804.1:n.1501+119_1501+120del
ENST00000544574.5:c.*383_*384del ENSP00000438565.1:n.*383_*384del
ENST00000560968.5:c.1318+119_1318+120del
ENST00000615446.4:c.289+119_289+120del ENSP00000483994.1:n.289+119_289+120del
ENST00000617366.4:c.618+119_618+120del ENSP00000481967.1:n.618+119_618+120del
NM_000545.5:c.1501+119_1501+120del , LRG_522t1:c.1501+119_1501+120del NP_000536.5:n.1501+119_1501+120del
NM_000545.6:c.1501+119_1501+120del NP_000536.5:n.1501+119_1501+120del
NM_001306179.1:c.1501+119_1501+120del NP_001293108.1:n.1501+119_1501+120del
XM_005253931.2:c.1501+119_1501+120del XP_005253988.1:n.1501+119_1501+120del
XM_024449168.1:c.1501+119_1501+120del XP_024304936.1:n.1501+119_1501+120del
NM_000545.8:c.1501+119_1501+120del MANE Select NP_000536.6:n.1501+119_1501+120del
NM_001306179.2:c.1501+119_1501+120del NP_001293108.2:n.1501+119_1501+120del