Canonical Allele Identifier: CA386970064
Gene: HNF1A HGNC NCBI

Linked Data

gnomAD v4: 12-120997518-A-G
MyVariant Identifiers: chr12:g.121435321A>G (hg19) chr12:g.120997518A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997518A>G , CM000674.2:g.120997518A>G GRCh38
NC_000012.11:g.121435321A>G , CM000674.1:g.121435321A>G GRCh37
NC_000012.10:g.119919704A>G NCBI36
NG_011731.2:g.23773A>G , LRG_522:g.23773A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*101A>G ENSP00000453965.2:n.*101A>G
ENST00000257555.11:c.1354A>G MANE Select ENSP00000257555.5:p.Met452Val
ENST00000257555.10:c.1354A>G ENSP00000257555.4:p.Met452Val
ENST00000400024.6:c.1354A>G ENSP00000476181.1:p.Met452Val
ENST00000402929.5:n.2220A>G
ENST00000535955.5:n.70A>G
ENST00000538626.2:n.218A>G
ENST00000538646.5:c.*330A>G ENSP00000443964.1:n.*330A>G
ENST00000540108.1:c.*794A>G ENSP00000445445.1:n.*794A>G
ENST00000541395.5:c.1354A>G ENSP00000443112.1:p.Met452Val
ENST00000541924.5:c.*368A>G ENSP00000440361.1:n.*368A>G
ENST00000543255.1:n.398A>G
ENST00000543427.5:c.817A>G ENSP00000439721.2:p.Met273Val
ENST00000544413.2:c.1354A>G ENSP00000438804.1:p.Met452Val
ENST00000544574.5:c.*117A>G ENSP00000438565.1:n.*117A>G
ENST00000560968.5:c.1171A>G
ENST00000615446.4:c.142A>G ENSP00000483994.1:p.Met48Val
ENST00000617366.4:c.587-116A>G ENSP00000481967.1:n.587-116A>G
NM_000545.5:c.1354A>G , LRG_522t1:c.1354A>G NP_000536.5:p.Met452Val
NM_000545.6:c.1354A>G NP_000536.5:p.Met452Val
NM_001306179.1:c.1354A>G NP_001293108.1:p.Met452Val
XM_005253931.2:c.1354A>G XP_005253988.1:p.Met452Val
XM_024449168.1:c.1354A>G XP_024304936.1:p.Met452Val
NM_000545.8:c.1354A>G MANE Select NP_000536.6:p.Met452Val
NM_001306179.2:c.1354A>G NP_001293108.2:p.Met452Val
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