Canonical Allele Identifier: CA2621382408
Gene: HNF1A HGNC NCBI

Linked Data

gnomAD v4: 12-120989070-G-GGCCCT
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120989070_120989071insGCCCT , CM000674.2:g.120989070_120989071insGCCCT GRCh38
NC_000012.11:g.121426873_121426874insGCCCT , CM000674.1:g.121426873_121426874insGCCCT GRCh37
NC_000012.10:g.119911256_119911257insGCCCT NCBI36
NG_011731.2:g.15325_15326insGCCCT , LRG_522:g.15325_15326insGCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.526+38_526+39insGCCCT ENSP00000453965.2:n.526+38_526+39insGCCCT
ENST00000257555.11:c.526+38_526+39insGCCCT MANE Select ENSP00000257555.5:n.526+38_526+39insGCCCT
ENST00000257555.10:c.526+38_526+39insGCCCT ENSP00000257555.4:n.526+38_526+39insGCCCT
ENST00000400024.6:c.526+38_526+39insGCCCT ENSP00000476181.1:n.526+38_526+39insGCCCT
ENST00000402929.5:n.661+38_661+39insGCCCT
ENST00000535955.5:n.43-8421_43-8420insGCCCT
ENST00000538626.2:n.191-8421_191-8420insGCCCT
ENST00000538646.5:c.526+38_526+39insGCCCT ENSP00000443964.1:n.526+38_526+39insGCCCT
ENST00000540108.1:c.327-4450_327-4449insGCCCT ENSP00000445445.1:n.327-4450_327-4449insGCCCT
ENST00000541395.5:c.526+38_526+39insGCCCT ENSP00000443112.1:n.526+38_526+39insGCCCT
ENST00000541924.5:c.526+38_526+39insGCCCT ENSP00000440361.1:n.526+38_526+39insGCCCT
ENST00000543427.5:c.526+38_526+39insGCCCT ENSP00000439721.2:n.526+38_526+39insGCCCT
ENST00000544413.2:c.526+38_526+39insGCCCT ENSP00000438804.1:n.526+38_526+39insGCCCT
ENST00000544574.5:c.73-7547_73-7546insGCCCT ENSP00000438565.1:n.73-7547_73-7546insGCCCT
ENST00000560968.5:c.669+38_669+39insGCCCT
ENST00000615446.4:c.-257-7192_-257-7191insGCCCT ENSP00000483994.1:n.-257-7192_-257-7191insGCCCT
ENST00000617366.4:c.526+38_526+39insGCCCT ENSP00000481967.1:n.526+38_526+39insGCCCT
NM_000545.5:c.526+38_526+39insGCCCT , LRG_522t1:c.526+38_526+39insGCCCT NP_000536.5:n.526+38_526+39insGCCCT
NM_000545.6:c.526+38_526+39insGCCCT NP_000536.5:n.526+38_526+39insGCCCT
NM_001306179.1:c.526+38_526+39insGCCCT NP_001293108.1:n.526+38_526+39insGCCCT
XM_005253931.2:c.526+38_526+39insGCCCT XP_005253988.1:n.526+38_526+39insGCCCT
XM_024449168.1:c.526+38_526+39insGCCCT XP_024304936.1:n.526+38_526+39insGCCCT
NM_000545.8:c.526+38_526+39insGCCCT MANE Select NP_000536.6:n.526+38_526+39insGCCCT
NM_001306179.2:c.526+38_526+39insGCCCT NP_001293108.2:n.526+38_526+39insGCCCT
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