Canonical Allele Identifier: CA386970144
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs2135847715
MyVariant Identifiers: chr12:g.121435357T>G (hg19) chr12:g.120997554T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997554T>G , CM000674.2:g.120997554T>G GRCh38
NC_000012.11:g.121435357T>G , CM000674.1:g.121435357T>G GRCh37
NC_000012.10:g.119919740T>G NCBI36
NG_011731.2:g.23809T>G , LRG_522:g.23809T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*137T>G ENSP00000453965.2:n.*137T>G
ENST00000257555.11:c.1390T>G MANE Select ENSP00000257555.5:p.Phe464Val
ENST00000257555.10:c.1390T>G ENSP00000257555.4:p.Phe464Val
ENST00000400024.6:c.1390T>G ENSP00000476181.1:p.Phe464Val
ENST00000402929.5:n.2256T>G
ENST00000535955.5:n.106T>G
ENST00000538626.2:n.254T>G
ENST00000538646.5:c.*366T>G ENSP00000443964.1:n.*366T>G
ENST00000540108.1:c.*830T>G ENSP00000445445.1:n.*830T>G
ENST00000541395.5:c.1390T>G ENSP00000443112.1:p.Phe464Val
ENST00000541924.5:c.*404T>G ENSP00000440361.1:n.*404T>G
ENST00000543255.1:n.434T>G
ENST00000543427.5:c.853T>G ENSP00000439721.2:p.Phe285Val
ENST00000544413.2:c.1390T>G ENSP00000438804.1:p.Phe464Val
ENST00000544574.5:c.*153T>G ENSP00000438565.1:n.*153T>G
ENST00000560968.5:c.1207T>G
ENST00000615446.4:c.178T>G ENSP00000483994.1:p.Phe60Val
ENST00000617366.4:c.587-80T>G ENSP00000481967.1:n.587-80T>G
NM_000545.5:c.1390T>G , LRG_522t1:c.1390T>G NP_000536.5:p.Phe464Val
NM_000545.6:c.1390T>G NP_000536.5:p.Phe464Val
NM_001306179.1:c.1390T>G NP_001293108.1:p.Phe464Val
XM_005253931.2:c.1390T>G XP_005253988.1:p.Phe464Val
XM_024449168.1:c.1390T>G XP_024304936.1:p.Phe464Val
NM_000545.8:c.1390T>G MANE Select NP_000536.6:p.Phe464Val
NM_001306179.2:c.1390T>G NP_001293108.2:p.Phe464Val
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