Canonical Allele Identifier: CA482165208
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs2135847870
MyVariant Identifiers: chr12:g.121435386G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997583G>A , CM000674.2:g.120997583G>A GRCh38
NC_000012.11:g.121435386G>A , CM000674.1:g.121435386G>A GRCh37
NC_000012.10:g.119919769G>A NCBI36
NG_011731.2:g.23838G>A , LRG_522:g.23838G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*166G>A ENSP00000453965.2:n.*166G>A
ENST00000257555.11:c.1419G>A MANE Select ENSP00000257555.5:p.Gln473=
ENST00000257555.10:c.1419G>A ENSP00000257555.4:p.Gln473=
ENST00000400024.6:c.1419G>A ENSP00000476181.1:p.Gln473=
ENST00000402929.5:n.2285G>A
ENST00000535955.5:n.135G>A
ENST00000538626.2:n.283G>A
ENST00000538646.5:c.*395G>A ENSP00000443964.1:n.*395G>A
ENST00000540108.1:c.*859G>A ENSP00000445445.1:n.*859G>A
ENST00000541395.5:c.1419G>A ENSP00000443112.1:p.Gln473=
ENST00000541924.5:c.*433G>A ENSP00000440361.1:n.*433G>A
ENST00000543255.1:n.463G>A
ENST00000543427.5:c.882G>A ENSP00000439721.2:p.Gln294=
ENST00000544413.2:c.1419G>A ENSP00000438804.1:p.Gln473=
ENST00000544574.5:c.*182G>A ENSP00000438565.1:n.*182G>A
ENST00000560968.5:c.1236G>A
ENST00000615446.4:c.207G>A ENSP00000483994.1:p.Gln69=
ENST00000617366.4:c.587-51G>A ENSP00000481967.1:n.587-51G>A
NM_000545.5:c.1419G>A , LRG_522t1:c.1419G>A NP_000536.5:p.Gln473=
NM_000545.6:c.1419G>A NP_000536.5:p.Gln473=
NM_001306179.1:c.1419G>A NP_001293108.1:p.Gln473=
XM_005253931.2:c.1419G>A XP_005253988.1:p.Gln473=
XM_024449168.1:c.1419G>A XP_024304936.1:p.Gln473=
NM_000545.8:c.1419G>A MANE Select NP_000536.6:p.Gln473=
NM_001306179.2:c.1419G>A NP_001293108.2:p.Gln473=