Canonical Allele Identifier: CA386966835
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs1408350148
gnomAD v2: 12-121432184-G-T
gnomAD v4: 12-120994381-G-T
MyVariant Identifiers: chr12:g.121432184G>T (hg19) chr12:g.120994381G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994381G>T , CM000674.2:g.120994381G>T GRCh38
NC_000012.11:g.121432184G>T , CM000674.1:g.121432184G>T GRCh37
NC_000012.10:g.119916567G>T NCBI36
NG_011731.2:g.20636G>T , LRG_522:g.20636G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+181G>T ENSP00000453965.2:n.750+181G>T
ENST00000257555.11:c.931G>T MANE Select ENSP00000257555.5:p.Ala311Ser
ENST00000257555.10:c.931G>T ENSP00000257555.4:p.Ala311Ser
ENST00000400024.6:c.931G>T ENSP00000476181.1:p.Ala311Ser
ENST00000402929.5:n.1066G>T
ENST00000535955.5:n.43-3110G>T
ENST00000538626.2:n.191-3110G>T
ENST00000538646.5:c.744G>T ENSP00000443964.1:p.Leu248=
ENST00000540108.1:c.*371G>T ENSP00000445445.1:n.*371G>T
ENST00000541395.5:c.931G>T ENSP00000443112.1:p.Ala311Ser
ENST00000541924.5:c.713+675G>T ENSP00000440361.1:n.713+675G>T
ENST00000543427.5:c.633+755G>T ENSP00000439721.2:n.633+755G>T
ENST00000544413.2:c.931G>T ENSP00000438804.1:p.Ala311Ser
ENST00000544574.5:c.73-2236G>T ENSP00000438565.1:n.73-2236G>T
ENST00000560968.5:c.893+181G>T
ENST00000615446.4:c.-257-1881G>T ENSP00000483994.1:n.-257-1881G>T
ENST00000617366.4:c.586+802G>T ENSP00000481967.1:n.586+802G>T
NM_000545.5:c.931G>T , LRG_522t1:c.931G>T NP_000536.5:p.Ala311Ser
NM_000545.6:c.931G>T NP_000536.5:p.Ala311Ser
NM_001306179.1:c.931G>T NP_001293108.1:p.Ala311Ser
XM_005253931.2:c.931G>T XP_005253988.1:p.Ala311Ser
XM_024449168.1:c.931G>T XP_024304936.1:p.Ala311Ser
NM_000545.8:c.931G>T MANE Select NP_000536.6:p.Ala311Ser
NM_001306179.2:c.931G>T NP_001293108.2:p.Ala311Ser
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