Canonical Allele Identifier: CA2067678627
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993750_120993751delinsCG , CM000674.2:g.120993750_120993751delinsCG GRCh38
NC_000012.11:g.121431553_121431554delinsCG , CM000674.1:g.121431553_121431554delinsCG GRCh37
NC_000012.10:g.119915936_119915937delinsCG NCBI36
NG_011731.2:g.20005_20006delinsCG , LRG_522:g.20005_20006delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.713+44_713+45delinsCG ENSP00000453965.2:n.713+44_713+45delinsCG
ENST00000257555.11:c.713+44_713+45delinsCG MANE Select ENSP00000257555.5:n.713+44_713+45delinsCG
ENST00000257555.10:c.713+44_713+45delinsCG ENSP00000257555.4:n.713+44_713+45delinsCG
ENST00000400024.6:c.713+44_713+45delinsCG ENSP00000476181.1:n.713+44_713+45delinsCG
ENST00000402929.5:n.848+44_848+45delinsCG
ENST00000535955.5:n.43-3741_43-3740delinsCG
ENST00000538626.2:n.191-3741_191-3740delinsCG
ENST00000538646.5:c.527-414_527-413delinsCG ENSP00000443964.1:n.527-414_527-413delinsCG
ENST00000540108.1:c.*153+44_*153+45delinsCG ENSP00000445445.1:n.*153+44_*153+45delinsCG
ENST00000541395.5:c.713+44_713+45delinsCG ENSP00000443112.1:n.713+44_713+45delinsCG
ENST00000541924.5:c.713+44_713+45delinsCG ENSP00000440361.1:n.713+44_713+45delinsCG
ENST00000543427.5:c.633+124_633+125delinsCG ENSP00000439721.2:n.633+124_633+125delinsCG
ENST00000544413.2:c.713+44_713+45delinsCG ENSP00000438804.1:n.713+44_713+45delinsCG
ENST00000544574.5:c.73-2867_73-2866delinsCG ENSP00000438565.1:n.73-2867_73-2866delinsCG
ENST00000560968.5:c.856+44_856+45delinsCG
ENST00000615446.4:c.-257-2512_-257-2511delinsCG ENSP00000483994.1:n.-257-2512_-257-2511delinsCG
ENST00000617366.4:c.586+171_586+172delinsCG ENSP00000481967.1:n.586+171_586+172delinsCG
NM_000545.5:c.713+44_713+45delinsCG , LRG_522t1:c.713+44_713+45delinsCG NP_000536.5:n.713+44_713+45delinsCG
NM_000545.6:c.713+44_713+45delinsCG NP_000536.5:n.713+44_713+45delinsCG
NM_001306179.1:c.713+44_713+45delinsCG NP_001293108.1:n.713+44_713+45delinsCG
XM_005253931.2:c.713+44_713+45delinsCG XP_005253988.1:n.713+44_713+45delinsCG
XM_024449168.1:c.713+44_713+45delinsCG XP_024304936.1:n.713+44_713+45delinsCG
NM_000545.8:c.713+44_713+45delinsCG MANE Select NP_000536.6:n.713+44_713+45delinsCG
NM_001306179.2:c.713+44_713+45delinsCG NP_001293108.2:n.713+44_713+45delinsCG