Canonical Allele Identifier: CA684422051
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs1216215605

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993792_120993793insCA , CM000674.2:g.120993792_120993793insCA GRCh38
NC_000012.11:g.121431595_121431596insCA , CM000674.1:g.121431595_121431596insCA GRCh37
NC_000012.10:g.119915978_119915979insCA NCBI36
NG_011731.2:g.20047_20048insCA , LRG_522:g.20047_20048insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.713+86_713+87insCA ENSP00000453965.2:n.713+86_713+87insCA
ENST00000257555.11:c.713+86_713+87insCA MANE Select ENSP00000257555.5:n.713+86_713+87insCA
ENST00000257555.10:c.713+86_713+87insCA ENSP00000257555.4:n.713+86_713+87insCA
ENST00000400024.6:c.713+86_713+87insCA ENSP00000476181.1:n.713+86_713+87insCA
ENST00000402929.5:n.848+86_848+87insCA
ENST00000535955.5:n.43-3699_43-3698insCA
ENST00000538626.2:n.191-3699_191-3698insCA
ENST00000538646.5:c.527-372_527-371insCA ENSP00000443964.1:n.527-372_527-371insCA
ENST00000540108.1:c.*153+86_*153+87insCA ENSP00000445445.1:n.*153+86_*153+87insCA
ENST00000541395.5:c.713+86_713+87insCA ENSP00000443112.1:n.713+86_713+87insCA
ENST00000541924.5:c.713+86_713+87insCA ENSP00000440361.1:n.713+86_713+87insCA
ENST00000543427.5:c.633+166_633+167insCA ENSP00000439721.2:n.633+166_633+167insCA
ENST00000544413.2:c.713+86_713+87insCA ENSP00000438804.1:n.713+86_713+87insCA
ENST00000544574.5:c.73-2825_73-2824insCA ENSP00000438565.1:n.73-2825_73-2824insCA
ENST00000560968.5:c.856+86_856+87insCA
ENST00000615446.4:c.-257-2470_-257-2469insCA ENSP00000483994.1:n.-257-2470_-257-2469insCA
ENST00000617366.4:c.586+213_586+214insCA ENSP00000481967.1:n.586+213_586+214insCA
NM_000545.5:c.713+86_713+87insCA , LRG_522t1:c.713+86_713+87insCA NP_000536.5:n.713+86_713+87insCA
NM_000545.6:c.713+86_713+87insCA NP_000536.5:n.713+86_713+87insCA
NM_001306179.1:c.713+86_713+87insCA NP_001293108.1:n.713+86_713+87insCA
XM_005253931.2:c.713+86_713+87insCA XP_005253988.1:n.713+86_713+87insCA
XM_024449168.1:c.713+86_713+87insCA XP_024304936.1:n.713+86_713+87insCA
NM_000545.8:c.713+86_713+87insCA MANE Select NP_000536.6:n.713+86_713+87insCA
NM_001306179.2:c.713+86_713+87insCA NP_001293108.2:n.713+86_713+87insCA