Canonical Allele Identifier: CA482164434
Gene: HNF1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121434175C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120996372C>T , CM000674.2:g.120996372C>T GRCh38
NC_000012.11:g.121434175C>T , CM000674.1:g.121434175C>T GRCh37
NC_000012.10:g.119918558C>T NCBI36
NG_011731.2:g.22627C>T , LRG_522:g.22627C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.751-11C>T ENSP00000453965.2:n.751-11C>T
ENST00000257555.11:c.1066C>T MANE Select ENSP00000257555.5:p.Leu356=
ENST00000257555.10:c.1066C>T ENSP00000257555.4:p.Leu356=
ENST00000400024.6:c.1066C>T ENSP00000476181.1:p.Leu356=
ENST00000402929.5:n.1201C>T
ENST00000535955.5:n.43-1119C>T
ENST00000538626.2:n.191-1119C>T
ENST00000538646.5:c.*42C>T ENSP00000443964.1:n.*42C>T
ENST00000540108.1:c.*506C>T ENSP00000445445.1:n.*506C>T
ENST00000541395.5:c.1066C>T ENSP00000443112.1:p.Leu356=
ENST00000541924.5:c.*80C>T ENSP00000440361.1:n.*80C>T
ENST00000543427.5:c.634-232C>T ENSP00000439721.2:n.634-232C>T
ENST00000544413.2:c.1066C>T ENSP00000438804.1:p.Leu356=
ENST00000544574.5:c.73-245C>T ENSP00000438565.1:n.73-245C>T
ENST00000560968.5:c.894-11C>T
ENST00000615446.4:c.-147C>T ENSP00000483994.1:n.-147C>T
ENST00000617366.4:c.587-1262C>T ENSP00000481967.1:n.587-1262C>T
NM_000545.5:c.1066C>T , LRG_522t1:c.1066C>T NP_000536.5:p.Leu356=
NM_000545.6:c.1066C>T NP_000536.5:p.Leu356=
NM_001306179.1:c.1066C>T NP_001293108.1:p.Leu356=
XM_005253931.2:c.1066C>T XP_005253988.1:p.Leu356=
XM_024449168.1:c.1066C>T XP_024304936.1:p.Leu356=
NM_000545.8:c.1066C>T MANE Select NP_000536.6:p.Leu356=
NM_001306179.2:c.1066C>T NP_001293108.2:p.Leu356=