Canonical Allele Identifier: CA2067672595
Gene: HNF1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120988820_120988821delinsTG , CM000674.2:g.120988820_120988821delinsTG GRCh38
NC_000012.11:g.121426623_121426624delinsTG , CM000674.1:g.121426623_121426624delinsTG GRCh37
NC_000012.10:g.119911006_119911007delinsTG NCBI36
NG_011731.2:g.15075_15076delinsTG , LRG_522:g.15075_15076delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.327-13_327-12delinsTG ENSP00000453965.2:n.327-13_327-12delinsTG
ENST00000257555.11:c.327-13_327-12delinsTG MANE Select ENSP00000257555.5:n.327-13_327-12delinsTG
ENST00000257555.10:c.327-13_327-12delinsTG ENSP00000257555.4:n.327-13_327-12delinsTG
ENST00000400024.6:c.327-13_327-12delinsTG ENSP00000476181.1:n.327-13_327-12delinsTG
ENST00000402929.5:n.462-13_462-12delinsTG
ENST00000535955.5:n.43-8671_43-8670delinsTG
ENST00000538626.2:n.191-8671_191-8670delinsTG
ENST00000538646.5:c.327-13_327-12delinsTG ENSP00000443964.1:n.327-13_327-12delinsTG
ENST00000540108.1:c.327-4700_327-4699delinsTG ENSP00000445445.1:n.327-4700_327-4699delinsTG
ENST00000541395.5:c.327-13_327-12delinsTG ENSP00000443112.1:n.327-13_327-12delinsTG
ENST00000541924.5:c.327-13_327-12delinsTG ENSP00000440361.1:n.327-13_327-12delinsTG
ENST00000543427.5:c.327-13_327-12delinsTG ENSP00000439721.2:n.327-13_327-12delinsTG
ENST00000544413.2:c.327-13_327-12delinsTG ENSP00000438804.1:n.327-13_327-12delinsTG
ENST00000544574.5:c.73-7797_73-7796delinsTG ENSP00000438565.1:n.73-7797_73-7796delinsTG
ENST00000560968.5:c.470-13_470-12delinsTG
ENST00000615446.4:c.-257-7442_-257-7441delinsTG ENSP00000483994.1:n.-257-7442_-257-7441delinsTG
ENST00000617366.4:c.327-13_327-12delinsTG ENSP00000481967.1:n.327-13_327-12delinsTG
NM_000545.5:c.327-13_327-12delinsTG , LRG_522t1:c.327-13_327-12delinsTG NP_000536.5:n.327-13_327-12delinsTG
NM_000545.6:c.327-13_327-12delinsTG NP_000536.5:n.327-13_327-12delinsTG
NM_001306179.1:c.327-13_327-12delinsTG NP_001293108.1:n.327-13_327-12delinsTG
XM_005253931.2:c.327-13_327-12delinsTG XP_005253988.1:n.327-13_327-12delinsTG
XM_024449168.1:c.327-13_327-12delinsTG XP_024304936.1:n.327-13_327-12delinsTG
NM_000545.8:c.327-13_327-12delinsTG MANE Select NP_000536.6:n.327-13_327-12delinsTG
NM_001306179.2:c.327-13_327-12delinsTG NP_001293108.2:n.327-13_327-12delinsTG
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