Canonical Allele Identifier: CA2621383968
Gene: HNF1A HGNC NCBI

Linked Data

gnomAD v4: 12-120994447-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994447A>G , CM000674.2:g.120994447A>G GRCh38
NC_000012.11:g.121432250A>G , CM000674.1:g.121432250A>G GRCh37
NC_000012.10:g.119916633A>G NCBI36
NG_011731.2:g.20702A>G , LRG_522:g.20702A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+247A>G ENSP00000453965.2:n.750+247A>G
ENST00000257555.11:c.955+42A>G MANE Select ENSP00000257555.5:n.955+42A>G
ENST00000257555.10:c.955+42A>G ENSP00000257555.4:n.955+42A>G
ENST00000400024.6:c.955+42A>G ENSP00000476181.1:n.955+42A>G
ENST00000402929.5:n.1090+42A>G
ENST00000535955.5:n.43-3044A>G
ENST00000538626.2:n.191-3044A>G
ENST00000538646.5:c.768+42A>G ENSP00000443964.1:n.768+42A>G
ENST00000540108.1:c.*395+42A>G ENSP00000445445.1:n.*395+42A>G
ENST00000541395.5:c.955+42A>G ENSP00000443112.1:n.955+42A>G
ENST00000541924.5:c.713+741A>G ENSP00000440361.1:n.713+741A>G
ENST00000543427.5:c.633+821A>G ENSP00000439721.2:n.633+821A>G
ENST00000544413.2:c.955+42A>G ENSP00000438804.1:n.955+42A>G
ENST00000544574.5:c.73-2170A>G ENSP00000438565.1:n.73-2170A>G
ENST00000560968.5:c.893+247A>G
ENST00000615446.4:c.-257-1815A>G ENSP00000483994.1:n.-257-1815A>G
ENST00000617366.4:c.586+868A>G ENSP00000481967.1:n.586+868A>G
NM_000545.5:c.955+42A>G , LRG_522t1:c.955+42A>G NP_000536.5:n.955+42A>G
NM_000545.6:c.955+42A>G NP_000536.5:n.955+42A>G
NM_001306179.1:c.955+42A>G NP_001293108.1:n.955+42A>G
XM_005253931.2:c.955+42A>G XP_005253988.1:n.955+42A>G
XM_024449168.1:c.955+42A>G XP_024304936.1:n.955+42A>G
NM_000545.8:c.955+42A>G MANE Select NP_000536.6:n.955+42A>G
NM_001306179.2:c.955+42A>G NP_001293108.2:n.955+42A>G
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