Canonical Allele Identifier: CA2621391158
Gene: HNF1A HGNC NCBI

Linked Data

gnomAD v4: 12-120997772-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997775del , CM000674.2:g.120997775del GRCh38
NC_000012.11:g.121435578del , CM000674.1:g.121435578del GRCh37
NC_000012.10:g.119919961del NCBI36
NG_011731.2:g.24030del , LRG_522:g.24030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+110del ENSP00000453965.2:n.*248+110del
ENST00000257555.11:c.1501+110del MANE Select ENSP00000257555.5:n.1501+110del
ENST00000257555.10:c.1501+110del ENSP00000257555.4:n.1501+110del
ENST00000400024.6:c.1611del ENSP00000476181.1:p.Thr538GlnfsTer7
ENST00000402929.5:n.2477del
ENST00000535955.5:n.327del
ENST00000538626.2:n.475del
ENST00000538646.5:c.*587del ENSP00000443964.1:n.*587del
ENST00000540108.1:c.*941+110del ENSP00000445445.1:n.*941+110del
ENST00000541395.5:c.1501+110del ENSP00000443112.1:n.1501+110del
ENST00000541924.5:c.*625del ENSP00000440361.1:n.*625del
ENST00000543255.1:n.655del
ENST00000543427.5:c.964+110del ENSP00000439721.2:n.964+110del
ENST00000544413.2:c.1501+110del ENSP00000438804.1:n.1501+110del
ENST00000544574.5:c.*374del ENSP00000438565.1:n.*374del
ENST00000560968.5:c.1318+110del
ENST00000615446.4:c.289+110del ENSP00000483994.1:n.289+110del
ENST00000617366.4:c.618+110del ENSP00000481967.1:n.618+110del
NM_000545.5:c.1501+110del , LRG_522t1:c.1501+110del NP_000536.5:n.1501+110del
NM_000545.6:c.1501+110del NP_000536.5:n.1501+110del
NM_001306179.1:c.1501+110del NP_001293108.1:n.1501+110del
XM_005253931.2:c.1501+110del XP_005253988.1:n.1501+110del
XM_024449168.1:c.1501+110del XP_024304936.1:n.1501+110del
NM_000545.8:c.1501+110del MANE Select NP_000536.6:n.1501+110del
NM_001306179.2:c.1501+110del NP_001293108.2:n.1501+110del
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