Canonical Allele Identifier: CA244532740
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs924513259

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993987_120993988del , CM000674.2:g.120993987_120993988del GRCh38
NC_000012.11:g.121431790_121431791del , CM000674.1:g.121431790_121431791del GRCh37
NC_000012.10:g.119916173_119916174del NCBI36
NG_011731.2:g.20242_20243del , LRG_522:g.20242_20243del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.714-177_714-176del ENSP00000453965.2:n.714-177_714-176del
ENST00000257555.11:c.714-177_714-176del MANE Select ENSP00000257555.5:n.714-177_714-176del
ENST00000257555.10:c.714-177_714-176del ENSP00000257555.4:n.714-177_714-176del
ENST00000400024.6:c.714-177_714-176del ENSP00000476181.1:n.714-177_714-176del
ENST00000402929.5:n.849-177_849-176del
ENST00000535955.5:n.43-3504_43-3503del
ENST00000538626.2:n.191-3504_191-3503del
ENST00000538646.5:c.527-177_527-176del ENSP00000443964.1:n.527-177_527-176del
ENST00000540108.1:c.*154-177_*154-176del ENSP00000445445.1:n.*154-177_*154-176del
ENST00000541395.5:c.714-177_714-176del ENSP00000443112.1:n.714-177_714-176del
ENST00000541924.5:c.713+281_713+282del ENSP00000440361.1:n.713+281_713+282del
ENST00000543427.5:c.633+361_633+362del ENSP00000439721.2:n.633+361_633+362del
ENST00000544413.2:c.714-177_714-176del ENSP00000438804.1:n.714-177_714-176del
ENST00000544574.5:c.73-2630_73-2629del ENSP00000438565.1:n.73-2630_73-2629del
ENST00000560968.5:c.857-177_857-176del
ENST00000615446.4:c.-257-2275_-257-2274del ENSP00000483994.1:n.-257-2275_-257-2274del
ENST00000617366.4:c.586+408_586+409del ENSP00000481967.1:n.586+408_586+409del
NM_000545.5:c.714-177_714-176del , LRG_522t1:c.714-177_714-176del NP_000536.5:n.714-177_714-176del
NM_000545.6:c.714-177_714-176del NP_000536.5:n.714-177_714-176del
NM_001306179.1:c.714-177_714-176del NP_001293108.1:n.714-177_714-176del
XM_005253931.2:c.714-177_714-176del XP_005253988.1:n.714-177_714-176del
XM_024449168.1:c.714-177_714-176del XP_024304936.1:n.714-177_714-176del
NM_000545.8:c.714-177_714-176del MANE Select NP_000536.6:n.714-177_714-176del
NM_001306179.2:c.714-177_714-176del NP_001293108.2:n.714-177_714-176del