Canonical Allele Identifier: CA386970246
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs2135847955
MyVariant Identifiers: chr12:g.121435403C>G (hg19) chr12:g.120997600C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997600C>G , CM000674.2:g.120997600C>G GRCh38
NC_000012.11:g.121435403C>G , CM000674.1:g.121435403C>G GRCh37
NC_000012.10:g.119919786C>G NCBI36
NG_011731.2:g.23855C>G , LRG_522:g.23855C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*183C>G ENSP00000453965.2:n.*183C>G
ENST00000257555.11:c.1436C>G MANE Select ENSP00000257555.5:p.Pro479Arg
ENST00000257555.10:c.1436C>G ENSP00000257555.4:p.Pro479Arg
ENST00000400024.6:c.1436C>G ENSP00000476181.1:p.Pro479Arg
ENST00000402929.5:n.2302C>G
ENST00000535955.5:n.152C>G
ENST00000538626.2:n.300C>G
ENST00000538646.5:c.*412C>G ENSP00000443964.1:n.*412C>G
ENST00000540108.1:c.*876C>G ENSP00000445445.1:n.*876C>G
ENST00000541395.5:c.1436C>G ENSP00000443112.1:p.Pro479Arg
ENST00000541924.5:c.*450C>G ENSP00000440361.1:n.*450C>G
ENST00000543255.1:n.480C>G
ENST00000543427.5:c.899C>G ENSP00000439721.2:p.Pro300Arg
ENST00000544413.2:c.1436C>G ENSP00000438804.1:p.Pro479Arg
ENST00000544574.5:c.*199C>G ENSP00000438565.1:n.*199C>G
ENST00000560968.5:c.1253C>G
ENST00000615446.4:c.224C>G ENSP00000483994.1:p.Pro75Arg
ENST00000617366.4:c.587-34C>G ENSP00000481967.1:n.587-34C>G
NM_000545.5:c.1436C>G , LRG_522t1:c.1436C>G NP_000536.5:p.Pro479Arg
NM_000545.6:c.1436C>G NP_000536.5:p.Pro479Arg
NM_001306179.1:c.1436C>G NP_001293108.1:p.Pro479Arg
XM_005253931.2:c.1436C>G XP_005253988.1:p.Pro479Arg
XM_024449168.1:c.1436C>G XP_024304936.1:p.Pro479Arg
NM_000545.8:c.1436C>G MANE Select NP_000536.6:p.Pro479Arg
NM_001306179.2:c.1436C>G NP_001293108.2:p.Pro479Arg
Search 100 bp 5'
Search 100 bp 3'