Canonical Allele Identifier: CA2621391190
Gene: HNF1A HGNC NCBI

Linked Data

gnomAD v4: 12-120997809-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997809G>T , CM000674.2:g.120997809G>T GRCh38
NC_000012.11:g.121435612G>T , CM000674.1:g.121435612G>T GRCh37
NC_000012.10:g.119919995G>T NCBI36
NG_011731.2:g.24064G>T , LRG_522:g.24064G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+144G>T ENSP00000453965.2:n.*248+144G>T
ENST00000257555.11:c.1501+144G>T MANE Select ENSP00000257555.5:n.1501+144G>T
ENST00000257555.10:c.1501+144G>T ENSP00000257555.4:n.1501+144G>T
ENST00000400024.6:c.*16G>T ENSP00000476181.1:n.*16G>T
ENST00000402929.5:n.2511G>T
ENST00000535955.5:n.361G>T
ENST00000538626.2:n.509G>T
ENST00000538646.5:c.*621G>T ENSP00000443964.1:n.*621G>T
ENST00000540108.1:c.*941+144G>T ENSP00000445445.1:n.*941+144G>T
ENST00000541395.5:c.1501+144G>T ENSP00000443112.1:n.1501+144G>T
ENST00000541924.5:c.*659G>T ENSP00000440361.1:n.*659G>T
ENST00000543255.1:n.689G>T
ENST00000543427.5:c.964+144G>T ENSP00000439721.2:n.964+144G>T
ENST00000544413.2:c.1501+144G>T ENSP00000438804.1:n.1501+144G>T
ENST00000544574.5:c.*408G>T ENSP00000438565.1:n.*408G>T
ENST00000560968.5:c.1318+144G>T
ENST00000615446.4:c.289+144G>T ENSP00000483994.1:n.289+144G>T
ENST00000617366.4:c.618+144G>T ENSP00000481967.1:n.618+144G>T
NM_000545.5:c.1501+144G>T , LRG_522t1:c.1501+144G>T NP_000536.5:n.1501+144G>T
NM_000545.6:c.1501+144G>T NP_000536.5:n.1501+144G>T
NM_001306179.1:c.1501+144G>T NP_001293108.1:n.1501+144G>T
XM_005253931.2:c.1501+144G>T XP_005253988.1:n.1501+144G>T
XM_024449168.1:c.1501+144G>T XP_024304936.1:n.1501+144G>T
NM_000545.8:c.1501+144G>T MANE Select NP_000536.6:n.1501+144G>T
NM_001306179.2:c.1501+144G>T NP_001293108.2:n.1501+144G>T
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