Canonical Allele Identifier: CA2067680081
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994552_120994556delinsGTTCA , CM000674.2:g.120994552_120994556delinsGTTCA GRCh38
NC_000012.11:g.121432355_121432359delinsGTTCA , CM000674.1:g.121432355_121432359delinsGTTCA GRCh37
NC_000012.10:g.119916738_119916742delinsGTTCA NCBI36
NG_011731.2:g.20807_20811delinsGTTCA , LRG_522:g.20807_20811delinsGTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+352_750+356delinsGTTCA ENSP00000453965.2:n.750+352_750+356delinsGTTCA
ENST00000257555.11:c.955+147_955+151delinsGTTCA MANE Select ENSP00000257555.5:n.955+147_955+151delinsGTTCA
ENST00000257555.10:c.955+147_955+151delinsGTTCA ENSP00000257555.4:n.955+147_955+151delinsGTTCA
ENST00000400024.6:c.955+147_955+151delinsGTTCA ENSP00000476181.1:n.955+147_955+151delinsGTTCA
ENST00000402929.5:n.1090+147_1090+151delinsGTTCA
ENST00000535955.5:n.43-2939_43-2935delinsGTTCA
ENST00000538626.2:n.191-2939_191-2935delinsGTTCA
ENST00000538646.5:c.768+147_768+151delinsGTTCA ENSP00000443964.1:n.768+147_768+151delinsGTTCA
ENST00000540108.1:c.*395+147_*395+151delinsGTTCA ENSP00000445445.1:n.*395+147_*395+151delinsGTTCA
ENST00000541395.5:c.955+147_955+151delinsGTTCA ENSP00000443112.1:n.955+147_955+151delinsGTTCA
ENST00000541924.5:c.713+846_713+850delinsGTTCA ENSP00000440361.1:n.713+846_713+850delinsGTTCA
ENST00000543427.5:c.633+926_633+930delinsGTTCA ENSP00000439721.2:n.633+926_633+930delinsGTTCA
ENST00000544413.2:c.955+147_955+151delinsGTTCA ENSP00000438804.1:n.955+147_955+151delinsGTTCA
ENST00000544574.5:c.73-2065_73-2061delinsGTTCA ENSP00000438565.1:n.73-2065_73-2061delinsGTTCA
ENST00000560968.5:c.893+352_893+356delinsGTTCA
ENST00000615446.4:c.-257-1710_-257-1706delinsGTTCA ENSP00000483994.1:n.-257-1710_-257-1706delinsGTTCA
ENST00000617366.4:c.586+973_586+977delinsGTTCA ENSP00000481967.1:n.586+973_586+977delinsGTTCA
NM_000545.5:c.955+147_955+151delinsGTTCA , LRG_522t1:c.955+147_955+151delinsGTTCA NP_000536.5:n.955+147_955+151delinsGTTCA
NM_000545.6:c.955+147_955+151delinsGTTCA NP_000536.5:n.955+147_955+151delinsGTTCA
NM_001306179.1:c.955+147_955+151delinsGTTCA NP_001293108.1:n.955+147_955+151delinsGTTCA
XM_005253931.2:c.955+147_955+151delinsGTTCA XP_005253988.1:n.955+147_955+151delinsGTTCA
XM_024449168.1:c.955+147_955+151delinsGTTCA XP_024304936.1:n.955+147_955+151delinsGTTCA
NM_000545.8:c.955+147_955+151delinsGTTCA MANE Select NP_000536.6:n.955+147_955+151delinsGTTCA
NM_001306179.2:c.955+147_955+151delinsGTTCA NP_001293108.2:n.955+147_955+151delinsGTTCA