Canonical Allele Identifier: CA2621391181
Gene: HNF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997802_120997811del , CM000674.2:g.120997802_120997811del GRCh38
NC_000012.11:g.121435605_121435614del , CM000674.1:g.121435605_121435614del GRCh37
NC_000012.10:g.119919988_119919997del NCBI36
NG_011731.2:g.24057_24066del , LRG_522:g.24057_24066del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+137_*248+146del ENSP00000453965.2:n.*248+137_*248+146del
ENST00000257555.11:c.1501+137_1501+146del MANE Select ENSP00000257555.5:n.1501+137_1501+146del
ENST00000257555.10:c.1501+137_1501+146del ENSP00000257555.4:n.1501+137_1501+146del
ENST00000400024.6:c.*9_*18del ENSP00000476181.1:n.*9_*18del
ENST00000402929.5:n.2504_2513del
ENST00000535955.5:n.354_363del
ENST00000538626.2:n.502_511del
ENST00000538646.5:c.*614_*623del ENSP00000443964.1:n.*614_*623del
ENST00000540108.1:c.*941+137_*941+146del ENSP00000445445.1:n.*941+137_*941+146del
ENST00000541395.5:c.1501+137_1501+146del ENSP00000443112.1:n.1501+137_1501+146del
ENST00000541924.5:c.*652_*661del ENSP00000440361.1:n.*652_*661del
ENST00000543255.1:n.682_691del
ENST00000543427.5:c.964+137_964+146del ENSP00000439721.2:n.964+137_964+146del
ENST00000544413.2:c.1501+137_1501+146del ENSP00000438804.1:n.1501+137_1501+146del
ENST00000544574.5:c.*401_*410del ENSP00000438565.1:n.*401_*410del
ENST00000560968.5:c.1318+137_1318+146del
ENST00000615446.4:c.289+137_289+146del ENSP00000483994.1:n.289+137_289+146del
ENST00000617366.4:c.618+137_618+146del ENSP00000481967.1:n.618+137_618+146del
NM_000545.5:c.1501+137_1501+146del , LRG_522t1:c.1501+137_1501+146del NP_000536.5:n.1501+137_1501+146del
NM_000545.6:c.1501+137_1501+146del NP_000536.5:n.1501+137_1501+146del
NM_001306179.1:c.1501+137_1501+146del NP_001293108.1:n.1501+137_1501+146del
XM_005253931.2:c.1501+137_1501+146del XP_005253988.1:n.1501+137_1501+146del
XM_024449168.1:c.1501+137_1501+146del XP_024304936.1:n.1501+137_1501+146del
NM_000545.8:c.1501+137_1501+146del MANE Select NP_000536.6:n.1501+137_1501+146del
NM_001306179.2:c.1501+137_1501+146del NP_001293108.2:n.1501+137_1501+146del