Canonical Allele Identifier: CA482165122
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs776169793
MyVariant Identifiers: chr12:g.121435308G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997505G>C , CM000674.2:g.120997505G>C GRCh38
NC_000012.11:g.121435308G>C , CM000674.1:g.121435308G>C GRCh37
NC_000012.10:g.119919691G>C NCBI36
NG_011731.2:g.23760G>C , LRG_522:g.23760G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*88G>C ENSP00000453965.2:n.*88G>C
ENST00000257555.11:c.1341G>C MANE Select ENSP00000257555.5:p.Pro447=
ENST00000257555.10:c.1341G>C ENSP00000257555.4:p.Pro447=
ENST00000400024.6:c.1341G>C ENSP00000476181.1:p.Pro447=
ENST00000402929.5:n.2207G>C
ENST00000535955.5:n.57G>C
ENST00000538626.2:n.205G>C
ENST00000538646.5:c.*317G>C ENSP00000443964.1:n.*317G>C
ENST00000540108.1:c.*781G>C ENSP00000445445.1:n.*781G>C
ENST00000541395.5:c.1341G>C ENSP00000443112.1:p.Pro447=
ENST00000541924.5:c.*355G>C ENSP00000440361.1:n.*355G>C
ENST00000543255.1:n.385G>C
ENST00000543427.5:c.804G>C ENSP00000439721.2:p.Pro268=
ENST00000544413.2:c.1341G>C ENSP00000438804.1:p.Pro447=
ENST00000544574.5:c.*104G>C ENSP00000438565.1:n.*104G>C
ENST00000560968.5:c.1158G>C
ENST00000615446.4:c.129G>C ENSP00000483994.1:p.Pro43=
ENST00000617366.4:c.587-129G>C ENSP00000481967.1:n.587-129G>C
NM_000545.5:c.1341G>C , LRG_522t1:c.1341G>C NP_000536.5:p.Pro447=
NM_000545.6:c.1341G>C NP_000536.5:p.Pro447=
NM_001306179.1:c.1341G>C NP_001293108.1:p.Pro447=
XM_005253931.2:c.1341G>C XP_005253988.1:p.Pro447=
XM_024449168.1:c.1341G>C XP_024304936.1:p.Pro447=
NM_000545.8:c.1341G>C MANE Select NP_000536.6:p.Pro447=
NM_001306179.2:c.1341G>C NP_001293108.2:p.Pro447=