Canonical Allele Identifier: CA386970120
Gene: HNF1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121435346A>G (hg19) chr12:g.120997543A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997543A>G , CM000674.2:g.120997543A>G GRCh38
NC_000012.11:g.121435346A>G , CM000674.1:g.121435346A>G GRCh37
NC_000012.10:g.119919729A>G NCBI36
NG_011731.2:g.23798A>G , LRG_522:g.23798A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*126A>G ENSP00000453965.2:n.*126A>G
ENST00000257555.11:c.1379A>G MANE Select ENSP00000257555.5:p.Gln460Arg
ENST00000257555.10:c.1379A>G ENSP00000257555.4:p.Gln460Arg
ENST00000400024.6:c.1379A>G ENSP00000476181.1:p.Gln460Arg
ENST00000402929.5:n.2245A>G
ENST00000535955.5:n.95A>G
ENST00000538626.2:n.243A>G
ENST00000538646.5:c.*355A>G ENSP00000443964.1:n.*355A>G
ENST00000540108.1:c.*819A>G ENSP00000445445.1:n.*819A>G
ENST00000541395.5:c.1379A>G ENSP00000443112.1:p.Gln460Arg
ENST00000541924.5:c.*393A>G ENSP00000440361.1:n.*393A>G
ENST00000543255.1:n.423A>G
ENST00000543427.5:c.842A>G ENSP00000439721.2:p.Gln281Arg
ENST00000544413.2:c.1379A>G ENSP00000438804.1:p.Gln460Arg
ENST00000544574.5:c.*142A>G ENSP00000438565.1:n.*142A>G
ENST00000560968.5:c.1196A>G
ENST00000615446.4:c.167A>G ENSP00000483994.1:p.Gln56Arg
ENST00000617366.4:c.587-91A>G ENSP00000481967.1:n.587-91A>G
NM_000545.5:c.1379A>G , LRG_522t1:c.1379A>G NP_000536.5:p.Gln460Arg
NM_000545.6:c.1379A>G NP_000536.5:p.Gln460Arg
NM_001306179.1:c.1379A>G NP_001293108.1:p.Gln460Arg
XM_005253931.2:c.1379A>G XP_005253988.1:p.Gln460Arg
XM_024449168.1:c.1379A>G XP_024304936.1:p.Gln460Arg
NM_000545.8:c.1379A>G MANE Select NP_000536.6:p.Gln460Arg
NM_001306179.2:c.1379A>G NP_001293108.2:p.Gln460Arg
Search 100 bp 5'
Search 100 bp 3'