Canonical Allele Identifier: CA2621384040
Gene: HNF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994519_120994569del , CM000674.2:g.120994519_120994569del GRCh38
NC_000012.11:g.121432322_121432372del , CM000674.1:g.121432322_121432372del GRCh37
NC_000012.10:g.119916705_119916755del NCBI36
NG_011731.2:g.20774_20824del , LRG_522:g.20774_20824del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+319_750+369del ENSP00000453965.2:n.750+319_750+369del
ENST00000257555.11:c.955+114_955+164del MANE Select ENSP00000257555.5:n.955+114_955+164del
ENST00000257555.10:c.955+114_955+164del ENSP00000257555.4:n.955+114_955+164del
ENST00000400024.6:c.955+114_955+164del ENSP00000476181.1:n.955+114_955+164del
ENST00000402929.5:n.1090+114_1090+164del
ENST00000535955.5:n.43-2972_43-2922del
ENST00000538626.2:n.191-2972_191-2922del
ENST00000538646.5:c.768+114_768+164del ENSP00000443964.1:n.768+114_768+164del
ENST00000540108.1:c.*395+114_*395+164del ENSP00000445445.1:n.*395+114_*395+164del
ENST00000541395.5:c.955+114_955+164del ENSP00000443112.1:n.955+114_955+164del
ENST00000541924.5:c.713+813_713+863del ENSP00000440361.1:n.713+813_713+863del
ENST00000543427.5:c.633+893_633+943del ENSP00000439721.2:n.633+893_633+943del
ENST00000544413.2:c.955+114_955+164del ENSP00000438804.1:n.955+114_955+164del
ENST00000544574.5:c.73-2098_73-2048del ENSP00000438565.1:n.73-2098_73-2048del
ENST00000560968.5:c.893+319_893+369del
ENST00000615446.4:c.-257-1743_-257-1693del ENSP00000483994.1:n.-257-1743_-257-1693del
ENST00000617366.4:c.586+940_586+990del ENSP00000481967.1:n.586+940_586+990del
NM_000545.5:c.955+114_955+164del , LRG_522t1:c.955+114_955+164del NP_000536.5:n.955+114_955+164del
NM_000545.6:c.955+114_955+164del NP_000536.5:n.955+114_955+164del
NM_001306179.1:c.955+114_955+164del NP_001293108.1:n.955+114_955+164del
XM_005253931.2:c.955+114_955+164del XP_005253988.1:n.955+114_955+164del
XM_024449168.1:c.955+114_955+164del XP_024304936.1:n.955+114_955+164del
NM_000545.8:c.955+114_955+164del MANE Select NP_000536.6:n.955+114_955+164del
NM_001306179.2:c.955+114_955+164del NP_001293108.2:n.955+114_955+164del