Canonical Allele Identifier: CA2621384177

Gene: HNF1A

Linked Data

• gnomAD v4: 12-120996239-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996239C>G , CM000674.2:g.120996239C>G	GRCh38
NC_000012.11:g.121434042C>G , CM000674.1:g.121434042C>G	GRCh37
NC_000012.10:g.119918425C>G	NCBI36
NG_011731.2:g.22494C>G , LRG_522:g.22494C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.751-144C>G	ENSP00000453965.2:n.751-144C>G
ENST00000257555.11:c.956-23C>G MANE Select	ENSP00000257555.5:n.956-23C>G
ENST00000257555.10:c.956-23C>G	ENSP00000257555.4:n.956-23C>G
ENST00000400024.6:c.956-23C>G	ENSP00000476181.1:n.956-23C>G
ENST00000402929.5:n.1091-23C>G
ENST00000535955.5:n.43-1252C>G
ENST00000538626.2:n.191-1252C>G
ENST00000538646.5:c.769-23C>G	ENSP00000443964.1:n.769-23C>G
ENST00000540108.1:c.*396-23C>G	ENSP00000445445.1:n.*396-23C>G
ENST00000541395.5:c.956-23C>G	ENSP00000443112.1:n.956-23C>G
ENST00000541924.5:c.714-23C>G	ENSP00000440361.1:n.714-23C>G
ENST00000543427.5:c.634-365C>G	ENSP00000439721.2:n.634-365C>G
ENST00000544413.2:c.956-23C>G	ENSP00000438804.1:n.956-23C>G
ENST00000544574.5:c.73-378C>G	ENSP00000438565.1:n.73-378C>G
ENST00000560968.5:c.894-144C>G
ENST00000615446.4:c.-257-23C>G	ENSP00000483994.1:n.-257-23C>G
ENST00000617366.4:c.587-1395C>G	ENSP00000481967.1:n.587-1395C>G
NM_000545.5:c.956-23C>G , LRG_522t1:c.956-23C>G	NP_000536.5:n.956-23C>G
NM_000545.6:c.956-23C>G	NP_000536.5:n.956-23C>G
NM_001306179.1:c.956-23C>G	NP_001293108.1:n.956-23C>G
XM_005253931.2:c.956-23C>G	XP_005253988.1:n.956-23C>G
XM_024449168.1:c.956-23C>G	XP_024304936.1:n.956-23C>G
NM_000545.8:c.956-23C>G MANE Select	NP_000536.6:n.956-23C>G
NM_001306179.2:c.956-23C>G	NP_001293108.2:n.956-23C>G