Canonical Allele Identifier: CA482163945
Gene: HNF1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121431331_121431332insA (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993529dup , CM000674.2:g.120993529dup GRCh38
NC_000012.11:g.121431332dup , CM000674.1:g.121431332dup GRCh37
NC_000012.10:g.119915715dup NCBI36
NG_011731.2:g.19784dup , LRG_522:g.19784dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.536dup ENSP00000453965.2:p.His179GlnfsTer9
ENST00000257555.11:c.536dup MANE Select ENSP00000257555.5:p.His179GlnfsTer9
ENST00000257555.10:c.536dup ENSP00000257555.4:p.His179GlnfsTer9
ENST00000400024.6:c.536dup ENSP00000476181.1:p.His179GlnfsTer9
ENST00000402929.5:n.671dup
ENST00000535955.5:n.43-3962dup
ENST00000538626.2:n.191-3962dup
ENST00000538646.5:c.527-635dup ENSP00000443964.1:n.527-635dup
ENST00000540108.1:c.336dup ENSP00000445445.1:p.Cys113MetfsTer7
ENST00000541395.5:c.536dup ENSP00000443112.1:p.His179GlnfsTer9
ENST00000541924.5:c.536dup ENSP00000440361.1:p.His179GlnfsTer9
ENST00000543427.5:c.536dup ENSP00000439721.2:p.His179GlnfsTer9
ENST00000544413.2:c.536dup ENSP00000438804.1:p.His179GlnfsTer9
ENST00000544574.5:c.73-3088dup ENSP00000438565.1:n.73-3088dup
ENST00000560968.5:c.679dup
ENST00000615446.4:c.-257-2733dup ENSP00000483994.1:n.-257-2733dup
ENST00000617366.4:c.536dup ENSP00000481967.1:p.His179GlnfsTer9
NM_000545.5:c.536dup , LRG_522t1:c.536dup NP_000536.5:p.His179GlnfsTer9
NM_000545.6:c.536dup NP_000536.5:p.His179GlnfsTer9
NM_001306179.1:c.536dup NP_001293108.1:p.His179GlnfsTer9
XM_005253931.2:c.536dup XP_005253988.1:p.His179GlnfsTer9
XM_024449168.1:c.536dup XP_024304936.1:p.His179GlnfsTer9
NM_000545.8:c.536dup MANE Select NP_000536.6:p.His179GlnfsTer9
NM_001306179.2:c.536dup NP_001293108.2:p.His179GlnfsTer9
Search 100 bp 5'
Search 100 bp 3'