Canonical Allele Identifier: CA386965901
Gene: HNF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1676716
ClinVar RCV Id: RCV002222113
dbSNP Id: rs2135841315

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994195T>C , CM000674.2:g.120994195T>C GRCh38
NC_000012.11:g.121431998T>C , CM000674.1:g.121431998T>C GRCh37
NC_000012.10:g.119916381T>C NCBI36
NG_011731.2:g.20450T>C , LRG_522:g.20450T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.745T>C ENSP00000453965.2:p.Ser249Pro
ENST00000257555.11:c.745T>C MANE Select ENSP00000257555.5:p.Ser249Pro
ENST00000257555.10:c.745T>C ENSP00000257555.4:p.Ser249Pro
ENST00000400024.6:c.745T>C ENSP00000476181.1:p.Ser249Pro
ENST00000402929.5:n.880T>C
ENST00000535955.5:n.43-3296T>C
ENST00000538626.2:n.191-3296T>C
ENST00000538646.5:c.558T>C ENSP00000443964.1:p.His186=
ENST00000540108.1:c.*185T>C ENSP00000445445.1:n.*185T>C
ENST00000541395.5:c.745T>C ENSP00000443112.1:p.Ser249Pro
ENST00000541924.5:c.713+489T>C ENSP00000440361.1:n.713+489T>C
ENST00000543427.5:c.633+569T>C ENSP00000439721.2:n.633+569T>C
ENST00000544413.2:c.745T>C ENSP00000438804.1:p.Ser249Pro
ENST00000544574.5:c.73-2422T>C ENSP00000438565.1:n.73-2422T>C
ENST00000560968.5:c.888T>C
ENST00000615446.4:c.-257-2067T>C ENSP00000483994.1:n.-257-2067T>C
ENST00000617366.4:c.586+616T>C ENSP00000481967.1:n.586+616T>C
NM_000545.5:c.745T>C , LRG_522t1:c.745T>C NP_000536.5:p.Ser249Pro
NM_000545.6:c.745T>C NP_000536.5:p.Ser249Pro
NM_001306179.1:c.745T>C NP_001293108.1:p.Ser249Pro
XM_005253931.2:c.745T>C XP_005253988.1:p.Ser249Pro
XM_024449168.1:c.745T>C XP_024304936.1:p.Ser249Pro
NM_000545.8:c.745T>C MANE Select NP_000536.6:p.Ser249Pro
NM_001306179.2:c.745T>C NP_001293108.2:p.Ser249Pro