Canonical Allele Identifier: CA645588003
Gene: HNF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994262_120994263insCGG , CM000674.2:g.120994262_120994263insCGG GRCh38
NC_000012.11:g.121432065_121432066insCGG , CM000674.1:g.121432065_121432066insCGG GRCh37
NC_000012.10:g.119916448_119916449insCGG NCBI36
NG_011731.2:g.20517_20518insCGG , LRG_522:g.20517_20518insCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+62_750+63insCGG ENSP00000453965.2:n.750+62_750+63insCGG
ENST00000257555.11:c.812_813insCGG MANE Select ENSP00000257555.5:p.Arg271_Arg272insGly
ENST00000257555.10:c.812_813insCGG ENSP00000257555.4:p.Arg271_Arg272insGly
ENST00000400024.6:c.812_813insCGG ENSP00000476181.1:p.Arg271_Arg272insGly
ENST00000402929.5:n.947_948insCGG
ENST00000535955.5:n.43-3229_43-3228insCGG
ENST00000538626.2:n.191-3229_191-3228insCGG
ENST00000538646.5:c.625_626insCGG ENSP00000443964.1:p.Thr208_Gly209insAla
ENST00000540108.1:c.*252_*253insCGG ENSP00000445445.1:n.*252_*253insCGG
ENST00000541395.5:c.812_813insCGG ENSP00000443112.1:p.Arg271_Arg272insGly
ENST00000541924.5:c.713+556_713+557insCGG ENSP00000440361.1:n.713+556_713+557insCGG
ENST00000543427.5:c.633+636_633+637insCGG ENSP00000439721.2:n.633+636_633+637insCGG
ENST00000544413.2:c.812_813insCGG ENSP00000438804.1:p.Arg271_Arg272insGly
ENST00000544574.5:c.73-2355_73-2354insCGG ENSP00000438565.1:n.73-2355_73-2354insCGG
ENST00000560968.5:c.893+62_893+63insCGG
ENST00000615446.4:c.-257-2000_-257-1999insCGG ENSP00000483994.1:n.-257-2000_-257-1999insCGG
ENST00000617366.4:c.586+683_586+684insCGG ENSP00000481967.1:n.586+683_586+684insCGG
NM_000545.5:c.812_813insCGG , LRG_522t1:c.812_813insCGG NP_000536.5:p.Arg271_Arg272insGly
NM_000545.6:c.812_813insCGG NP_000536.5:p.Arg271_Arg272insGly
NM_001306179.1:c.812_813insCGG NP_001293108.1:p.Arg271_Arg272insGly
XM_005253931.2:c.812_813insCGG XP_005253988.1:p.Arg271_Arg272insGly
XM_024449168.1:c.812_813insCGG XP_024304936.1:p.Arg271_Arg272insGly
NM_000545.8:c.812_813insCGG MANE Select NP_000536.6:p.Arg271_Arg272insGly
NM_001306179.2:c.812_813insCGG NP_001293108.2:p.Arg271_Arg272insGly