Canonical Allele Identifier: CA2621391167
Gene: HNF1A HGNC NCBI

Linked Data

gnomAD v4: 12-120997794-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997794T>A , CM000674.2:g.120997794T>A GRCh38
NC_000012.11:g.121435597T>A , CM000674.1:g.121435597T>A GRCh37
NC_000012.10:g.119919980T>A NCBI36
NG_011731.2:g.24049T>A , LRG_522:g.24049T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+129T>A ENSP00000453965.2:n.*248+129T>A
ENST00000257555.11:c.1501+129T>A MANE Select ENSP00000257555.5:n.1501+129T>A
ENST00000257555.10:c.1501+129T>A ENSP00000257555.4:n.1501+129T>A
ENST00000400024.6:c.*1T>A ENSP00000476181.1:n.*1T>A
ENST00000402929.5:n.2496T>A
ENST00000535955.5:n.346T>A
ENST00000538626.2:n.494T>A
ENST00000538646.5:c.*606T>A ENSP00000443964.1:n.*606T>A
ENST00000540108.1:c.*941+129T>A ENSP00000445445.1:n.*941+129T>A
ENST00000541395.5:c.1501+129T>A ENSP00000443112.1:n.1501+129T>A
ENST00000541924.5:c.*644T>A ENSP00000440361.1:n.*644T>A
ENST00000543255.1:n.674T>A
ENST00000543427.5:c.964+129T>A ENSP00000439721.2:n.964+129T>A
ENST00000544413.2:c.1501+129T>A ENSP00000438804.1:n.1501+129T>A
ENST00000544574.5:c.*393T>A ENSP00000438565.1:n.*393T>A
ENST00000560968.5:c.1318+129T>A
ENST00000615446.4:c.289+129T>A ENSP00000483994.1:n.289+129T>A
ENST00000617366.4:c.618+129T>A ENSP00000481967.1:n.618+129T>A
NM_000545.5:c.1501+129T>A , LRG_522t1:c.1501+129T>A NP_000536.5:n.1501+129T>A
NM_000545.6:c.1501+129T>A NP_000536.5:n.1501+129T>A
NM_001306179.1:c.1501+129T>A NP_001293108.1:n.1501+129T>A
XM_005253931.2:c.1501+129T>A XP_005253988.1:n.1501+129T>A
XM_024449168.1:c.1501+129T>A XP_024304936.1:n.1501+129T>A
NM_000545.8:c.1501+129T>A MANE Select NP_000536.6:n.1501+129T>A
NM_001306179.2:c.1501+129T>A NP_001293108.2:n.1501+129T>A
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