Canonical Allele Identifier: CA2067680082
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs1876994525

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994558_120994561del , CM000674.2:g.120994558_120994561del GRCh38
NC_000012.11:g.121432361_121432364del , CM000674.1:g.121432361_121432364del GRCh37
NC_000012.10:g.119916744_119916747del NCBI36
NG_011731.2:g.20813_20816del , LRG_522:g.20813_20816del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+358_750+361del ENSP00000453965.2:n.750+358_750+361del
ENST00000257555.11:c.955+153_955+156del MANE Select ENSP00000257555.5:n.955+153_955+156del
ENST00000257555.10:c.955+153_955+156del ENSP00000257555.4:n.955+153_955+156del
ENST00000400024.6:c.955+153_955+156del ENSP00000476181.1:n.955+153_955+156del
ENST00000402929.5:n.1090+153_1090+156del
ENST00000535955.5:n.43-2933_43-2930del
ENST00000538626.2:n.191-2933_191-2930del
ENST00000538646.5:c.768+153_768+156del ENSP00000443964.1:n.768+153_768+156del
ENST00000540108.1:c.*395+153_*395+156del ENSP00000445445.1:n.*395+153_*395+156del
ENST00000541395.5:c.955+153_955+156del ENSP00000443112.1:n.955+153_955+156del
ENST00000541924.5:c.713+852_713+855del ENSP00000440361.1:n.713+852_713+855del
ENST00000543427.5:c.633+932_633+935del ENSP00000439721.2:n.633+932_633+935del
ENST00000544413.2:c.955+153_955+156del ENSP00000438804.1:n.955+153_955+156del
ENST00000544574.5:c.73-2059_73-2056del ENSP00000438565.1:n.73-2059_73-2056del
ENST00000560968.5:c.893+358_893+361del
ENST00000615446.4:c.-257-1704_-257-1701del ENSP00000483994.1:n.-257-1704_-257-1701del
ENST00000617366.4:c.586+979_586+982del ENSP00000481967.1:n.586+979_586+982del
NM_000545.5:c.955+153_955+156del , LRG_522t1:c.955+153_955+156del NP_000536.5:n.955+153_955+156del
NM_000545.6:c.955+153_955+156del NP_000536.5:n.955+153_955+156del
NM_001306179.1:c.955+153_955+156del NP_001293108.1:n.955+153_955+156del
XM_005253931.2:c.955+153_955+156del XP_005253988.1:n.955+153_955+156del
XM_024449168.1:c.955+153_955+156del XP_024304936.1:n.955+153_955+156del
NM_000545.8:c.955+153_955+156del MANE Select NP_000536.6:n.955+153_955+156del
NM_001306179.2:c.955+153_955+156del NP_001293108.2:n.955+153_955+156del