Canonical Allele Identifier: CA2067678932
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993986_120993988delinsCTG , CM000674.2:g.120993986_120993988delinsCTG GRCh38
NC_000012.11:g.121431789_121431791delinsCTG , CM000674.1:g.121431789_121431791delinsCTG GRCh37
NC_000012.10:g.119916172_119916174delinsCTG NCBI36
NG_011731.2:g.20241_20243delinsCTG , LRG_522:g.20241_20243delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.714-178_714-176delinsCTG ENSP00000453965.2:n.714-178_714-176delinsCTG
ENST00000257555.11:c.714-178_714-176delinsCTG MANE Select ENSP00000257555.5:n.714-178_714-176delinsCTG
ENST00000257555.10:c.714-178_714-176delinsCTG ENSP00000257555.4:n.714-178_714-176delinsCTG
ENST00000400024.6:c.714-178_714-176delinsCTG ENSP00000476181.1:n.714-178_714-176delinsCTG
ENST00000402929.5:n.849-178_849-176delinsCTG
ENST00000535955.5:n.43-3505_43-3503delinsCTG
ENST00000538626.2:n.191-3505_191-3503delinsCTG
ENST00000538646.5:c.527-178_527-176delinsCTG ENSP00000443964.1:n.527-178_527-176delinsCTG
ENST00000540108.1:c.*154-178_*154-176delinsCTG ENSP00000445445.1:n.*154-178_*154-176delinsCTG
ENST00000541395.5:c.714-178_714-176delinsCTG ENSP00000443112.1:n.714-178_714-176delinsCTG
ENST00000541924.5:c.713+280_713+282delinsCTG ENSP00000440361.1:n.713+280_713+282delinsCTG
ENST00000543427.5:c.633+360_633+362delinsCTG ENSP00000439721.2:n.633+360_633+362delinsCTG
ENST00000544413.2:c.714-178_714-176delinsCTG ENSP00000438804.1:n.714-178_714-176delinsCTG
ENST00000544574.5:c.73-2631_73-2629delinsCTG ENSP00000438565.1:n.73-2631_73-2629delinsCTG
ENST00000560968.5:c.857-178_857-176delinsCTG
ENST00000615446.4:c.-257-2276_-257-2274delinsCTG ENSP00000483994.1:n.-257-2276_-257-2274delinsCTG
ENST00000617366.4:c.586+407_586+409delinsCTG ENSP00000481967.1:n.586+407_586+409delinsCTG
NM_000545.5:c.714-178_714-176delinsCTG , LRG_522t1:c.714-178_714-176delinsCTG NP_000536.5:n.714-178_714-176delinsCTG
NM_000545.6:c.714-178_714-176delinsCTG NP_000536.5:n.714-178_714-176delinsCTG
NM_001306179.1:c.714-178_714-176delinsCTG NP_001293108.1:n.714-178_714-176delinsCTG
XM_005253931.2:c.714-178_714-176delinsCTG XP_005253988.1:n.714-178_714-176delinsCTG
XM_024449168.1:c.714-178_714-176delinsCTG XP_024304936.1:n.714-178_714-176delinsCTG
NM_000545.8:c.714-178_714-176delinsCTG MANE Select NP_000536.6:n.714-178_714-176delinsCTG
NM_001306179.2:c.714-178_714-176delinsCTG NP_001293108.2:n.714-178_714-176delinsCTG