Canonical Allele Identifier: CA2067682795

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996249_120996250delinsCT , CM000674.2:g.120996249_120996250delinsCT	GRCh38
NC_000012.11:g.121434052_121434053delinsCT , CM000674.1:g.121434052_121434053delinsCT	GRCh37
NC_000012.10:g.119918435_119918436delinsCT	NCBI36
NG_011731.2:g.22504_22505delinsCT , LRG_522:g.22504_22505delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.751-134_751-133delinsCT	ENSP00000453965.2:n.751-134_751-133delinsCT
ENST00000257555.11:c.956-13_956-12delinsCT MANE Select	ENSP00000257555.5:n.956-13_956-12delinsCT
ENST00000257555.10:c.956-13_956-12delinsCT	ENSP00000257555.4:n.956-13_956-12delinsCT
ENST00000400024.6:c.956-13_956-12delinsCT	ENSP00000476181.1:n.956-13_956-12delinsCT
ENST00000402929.5:n.1091-13_1091-12delinsCT
ENST00000535955.5:n.43-1242_43-1241delinsCT
ENST00000538626.2:n.191-1242_191-1241delinsCT
ENST00000538646.5:c.769-13_769-12delinsCT	ENSP00000443964.1:n.769-13_769-12delinsCT
ENST00000540108.1:c.*396-13_*396-12delinsCT	ENSP00000445445.1:n.*396-13_*396-12delinsCT
ENST00000541395.5:c.956-13_956-12delinsCT	ENSP00000443112.1:n.956-13_956-12delinsCT
ENST00000541924.5:c.714-13_714-12delinsCT	ENSP00000440361.1:n.714-13_714-12delinsCT
ENST00000543427.5:c.634-355_634-354delinsCT	ENSP00000439721.2:n.634-355_634-354delinsCT
ENST00000544413.2:c.956-13_956-12delinsCT	ENSP00000438804.1:n.956-13_956-12delinsCT
ENST00000544574.5:c.73-368_73-367delinsCT	ENSP00000438565.1:n.73-368_73-367delinsCT
ENST00000560968.5:c.894-134_894-133delinsCT
ENST00000615446.4:c.-257-13_-257-12delinsCT	ENSP00000483994.1:n.-257-13_-257-12delinsCT
ENST00000617366.4:c.587-1385_587-1384delinsCT	ENSP00000481967.1:n.587-1385_587-1384delinsCT
NM_000545.5:c.956-13_956-12delinsCT , LRG_522t1:c.956-13_956-12delinsCT	NP_000536.5:n.956-13_956-12delinsCT
NM_000545.6:c.956-13_956-12delinsCT	NP_000536.5:n.956-13_956-12delinsCT
NM_001306179.1:c.956-13_956-12delinsCT	NP_001293108.1:n.956-13_956-12delinsCT
XM_005253931.2:c.956-13_956-12delinsCT	XP_005253988.1:n.956-13_956-12delinsCT
XM_024449168.1:c.956-13_956-12delinsCT	XP_024304936.1:n.956-13_956-12delinsCT
NM_000545.8:c.956-13_956-12delinsCT MANE Select	NP_000536.6:n.956-13_956-12delinsCT
NM_001306179.2:c.956-13_956-12delinsCT	NP_001293108.2:n.956-13_956-12delinsCT