Canonical Allele Identifier: CA2067678718
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993813_120993816delinsACTC , CM000674.2:g.120993813_120993816delinsACTC GRCh38
NC_000012.11:g.121431616_121431619delinsACTC , CM000674.1:g.121431616_121431619delinsACTC GRCh37
NC_000012.10:g.119915999_119916002delinsACTC NCBI36
NG_011731.2:g.20068_20071delinsACTC , LRG_522:g.20068_20071delinsACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.713+107_713+110delinsACTC ENSP00000453965.2:n.713+107_713+110delinsACTC
ENST00000257555.11:c.713+107_713+110delinsACTC MANE Select ENSP00000257555.5:n.713+107_713+110delinsACTC
ENST00000257555.10:c.713+107_713+110delinsACTC ENSP00000257555.4:n.713+107_713+110delinsACTC
ENST00000400024.6:c.713+107_713+110delinsACTC ENSP00000476181.1:n.713+107_713+110delinsACTC
ENST00000402929.5:n.848+107_848+110delinsACTC
ENST00000535955.5:n.43-3678_43-3675delinsACTC
ENST00000538626.2:n.191-3678_191-3675delinsACTC
ENST00000538646.5:c.527-351_527-348delinsACTC ENSP00000443964.1:n.527-351_527-348delinsACTC
ENST00000540108.1:c.*153+107_*153+110delinsACTC ENSP00000445445.1:n.*153+107_*153+110delinsACTC
ENST00000541395.5:c.713+107_713+110delinsACTC ENSP00000443112.1:n.713+107_713+110delinsACTC
ENST00000541924.5:c.713+107_713+110delinsACTC ENSP00000440361.1:n.713+107_713+110delinsACTC
ENST00000543427.5:c.633+187_633+190delinsACTC ENSP00000439721.2:n.633+187_633+190delinsACTC
ENST00000544413.2:c.713+107_713+110delinsACTC ENSP00000438804.1:n.713+107_713+110delinsACTC
ENST00000544574.5:c.73-2804_73-2801delinsACTC ENSP00000438565.1:n.73-2804_73-2801delinsACTC
ENST00000560968.5:c.856+107_856+110delinsACTC
ENST00000615446.4:c.-257-2449_-257-2446delinsACTC ENSP00000483994.1:n.-257-2449_-257-2446delinsACTC
ENST00000617366.4:c.586+234_586+237delinsACTC ENSP00000481967.1:n.586+234_586+237delinsACTC
NM_000545.5:c.713+107_713+110delinsACTC , LRG_522t1:c.713+107_713+110delinsACTC NP_000536.5:n.713+107_713+110delinsACTC
NM_000545.6:c.713+107_713+110delinsACTC NP_000536.5:n.713+107_713+110delinsACTC
NM_001306179.1:c.713+107_713+110delinsACTC NP_001293108.1:n.713+107_713+110delinsACTC
XM_005253931.2:c.713+107_713+110delinsACTC XP_005253988.1:n.713+107_713+110delinsACTC
XM_024449168.1:c.713+107_713+110delinsACTC XP_024304936.1:n.713+107_713+110delinsACTC
NM_000545.8:c.713+107_713+110delinsACTC MANE Select NP_000536.6:n.713+107_713+110delinsACTC
NM_001306179.2:c.713+107_713+110delinsACTC NP_001293108.2:n.713+107_713+110delinsACTC