Canonical Allele Identifier: CA2727245156
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs2135843022

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994517_120994521del , CM000674.2:g.120994517_120994521del GRCh38
NC_000012.11:g.121432320_121432324del , CM000674.1:g.121432320_121432324del GRCh37
NC_000012.10:g.119916703_119916707del NCBI36
NG_011731.2:g.20772_20776del , LRG_522:g.20772_20776del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+317_750+321del ENSP00000453965.2:n.750+317_750+321del
ENST00000257555.11:c.955+112_955+116del MANE Select ENSP00000257555.5:n.955+112_955+116del
ENST00000257555.10:c.955+112_955+116del ENSP00000257555.4:n.955+112_955+116del
ENST00000400024.6:c.955+112_955+116del ENSP00000476181.1:n.955+112_955+116del
ENST00000402929.5:n.1090+112_1090+116del
ENST00000535955.5:n.43-2974_43-2970del
ENST00000538626.2:n.191-2974_191-2970del
ENST00000538646.5:c.768+112_768+116del ENSP00000443964.1:n.768+112_768+116del
ENST00000540108.1:c.*395+112_*395+116del ENSP00000445445.1:n.*395+112_*395+116del
ENST00000541395.5:c.955+112_955+116del ENSP00000443112.1:n.955+112_955+116del
ENST00000541924.5:c.713+811_713+815del ENSP00000440361.1:n.713+811_713+815del
ENST00000543427.5:c.633+891_633+895del ENSP00000439721.2:n.633+891_633+895del
ENST00000544413.2:c.955+112_955+116del ENSP00000438804.1:n.955+112_955+116del
ENST00000544574.5:c.73-2100_73-2096del ENSP00000438565.1:n.73-2100_73-2096del
ENST00000560968.5:c.893+317_893+321del
ENST00000615446.4:c.-257-1745_-257-1741del ENSP00000483994.1:n.-257-1745_-257-1741del
ENST00000617366.4:c.586+938_586+942del ENSP00000481967.1:n.586+938_586+942del
NM_000545.5:c.955+112_955+116del , LRG_522t1:c.955+112_955+116del NP_000536.5:n.955+112_955+116del
NM_000545.6:c.955+112_955+116del NP_000536.5:n.955+112_955+116del
NM_001306179.1:c.955+112_955+116del NP_001293108.1:n.955+112_955+116del
XM_005253931.2:c.955+112_955+116del XP_005253988.1:n.955+112_955+116del
XM_024449168.1:c.955+112_955+116del XP_024304936.1:n.955+112_955+116del
NM_000545.8:c.955+112_955+116del MANE Select NP_000536.6:n.955+112_955+116del
NM_001306179.2:c.955+112_955+116del NP_001293108.2:n.955+112_955+116del