Canonical Allele Identifier: CA607888307
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs1379190492

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997822_120997833del , CM000674.2:g.120997822_120997833del GRCh38
NC_000012.11:g.121435625_121435636del , CM000674.1:g.121435625_121435636del GRCh37
NC_000012.10:g.119920008_119920019del NCBI36
NG_011731.2:g.24077_24088del , LRG_522:g.24077_24088del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+157_*248+168del ENSP00000453965.2:n.*248+157_*248+168del
ENST00000257555.11:c.1501+157_1501+168del MANE Select ENSP00000257555.5:n.1501+157_1501+168del
ENST00000257555.10:c.1501+157_1501+168del ENSP00000257555.4:n.1501+157_1501+168del
ENST00000400024.6:c.*29_*40del ENSP00000476181.1:n.*29_*40del
ENST00000402929.5:n.2524_2535del
ENST00000535955.5:n.374_385del
ENST00000538626.2:n.522_533del
ENST00000538646.5:c.*634_*645del ENSP00000443964.1:n.*634_*645del
ENST00000540108.1:c.*941+157_*941+168del ENSP00000445445.1:n.*941+157_*941+168del
ENST00000541395.5:c.1501+157_1501+168del ENSP00000443112.1:n.1501+157_1501+168del
ENST00000541924.5:c.*672_*683del ENSP00000440361.1:n.*672_*683del
ENST00000543255.1:n.702_713del
ENST00000543427.5:c.964+157_964+168del ENSP00000439721.2:n.964+157_964+168del
ENST00000544413.2:c.1501+157_1501+168del ENSP00000438804.1:n.1501+157_1501+168del
ENST00000544574.5:c.*421_*432del ENSP00000438565.1:n.*421_*432del
ENST00000560968.5:c.1318+157_1318+168del
ENST00000615446.4:c.289+157_289+168del ENSP00000483994.1:n.289+157_289+168del
ENST00000617366.4:c.618+157_618+168del ENSP00000481967.1:n.618+157_618+168del
NM_000545.5:c.1501+157_1501+168del , LRG_522t1:c.1501+157_1501+168del NP_000536.5:n.1501+157_1501+168del
NM_000545.6:c.1501+157_1501+168del NP_000536.5:n.1501+157_1501+168del
NM_001306179.1:c.1501+157_1501+168del NP_001293108.1:n.1501+157_1501+168del
XM_005253931.2:c.1501+157_1501+168del XP_005253988.1:n.1501+157_1501+168del
XM_024449168.1:c.1501+157_1501+168del XP_024304936.1:n.1501+157_1501+168del
NM_000545.8:c.1501+157_1501+168del MANE Select NP_000536.6:n.1501+157_1501+168del
NM_001306179.2:c.1501+157_1501+168del NP_001293108.2:n.1501+157_1501+168del