Canonical Allele Identifier: CA2067680025
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994457_120994458delinsAG , CM000674.2:g.120994457_120994458delinsAG GRCh38
NC_000012.11:g.121432260_121432261delinsAG , CM000674.1:g.121432260_121432261delinsAG GRCh37
NC_000012.10:g.119916643_119916644delinsAG NCBI36
NG_011731.2:g.20712_20713delinsAG , LRG_522:g.20712_20713delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+257_750+258delinsAG ENSP00000453965.2:n.750+257_750+258delinsAG
ENST00000257555.11:c.955+52_955+53delinsAG MANE Select ENSP00000257555.5:n.955+52_955+53delinsAG
ENST00000257555.10:c.955+52_955+53delinsAG ENSP00000257555.4:n.955+52_955+53delinsAG
ENST00000400024.6:c.955+52_955+53delinsAG ENSP00000476181.1:n.955+52_955+53delinsAG
ENST00000402929.5:n.1090+52_1090+53delinsAG
ENST00000535955.5:n.43-3034_43-3033delinsAG
ENST00000538626.2:n.191-3034_191-3033delinsAG
ENST00000538646.5:c.768+52_768+53delinsAG ENSP00000443964.1:n.768+52_768+53delinsAG
ENST00000540108.1:c.*395+52_*395+53delinsAG ENSP00000445445.1:n.*395+52_*395+53delinsAG
ENST00000541395.5:c.955+52_955+53delinsAG ENSP00000443112.1:n.955+52_955+53delinsAG
ENST00000541924.5:c.713+751_713+752delinsAG ENSP00000440361.1:n.713+751_713+752delinsAG
ENST00000543427.5:c.633+831_633+832delinsAG ENSP00000439721.2:n.633+831_633+832delinsAG
ENST00000544413.2:c.955+52_955+53delinsAG ENSP00000438804.1:n.955+52_955+53delinsAG
ENST00000544574.5:c.73-2160_73-2159delinsAG ENSP00000438565.1:n.73-2160_73-2159delinsAG
ENST00000560968.5:c.893+257_893+258delinsAG
ENST00000615446.4:c.-257-1805_-257-1804delinsAG ENSP00000483994.1:n.-257-1805_-257-1804delinsAG
ENST00000617366.4:c.586+878_586+879delinsAG ENSP00000481967.1:n.586+878_586+879delinsAG
NM_000545.5:c.955+52_955+53delinsAG , LRG_522t1:c.955+52_955+53delinsAG NP_000536.5:n.955+52_955+53delinsAG
NM_000545.6:c.955+52_955+53delinsAG NP_000536.5:n.955+52_955+53delinsAG
NM_001306179.1:c.955+52_955+53delinsAG NP_001293108.1:n.955+52_955+53delinsAG
XM_005253931.2:c.955+52_955+53delinsAG XP_005253988.1:n.955+52_955+53delinsAG
XM_024449168.1:c.955+52_955+53delinsAG XP_024304936.1:n.955+52_955+53delinsAG
NM_000545.8:c.955+52_955+53delinsAG MANE Select NP_000536.6:n.955+52_955+53delinsAG
NM_001306179.2:c.955+52_955+53delinsAG NP_001293108.2:n.955+52_955+53delinsAG