Canonical Allele Identifier: CA482164388

Gene: HNF1A

Linked Data

• MyVariant Identifiers: chr12:g.121434123C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996320C>A , CM000674.2:g.120996320C>A	GRCh38
NC_000012.11:g.121434123C>A , CM000674.1:g.121434123C>A	GRCh37
NC_000012.10:g.119918506C>A	NCBI36
NG_011731.2:g.22575C>A , LRG_522:g.22575C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.751-63C>A	ENSP00000453965.2:n.751-63C>A
ENST00000257555.11:c.1014C>A MANE Select	ENSP00000257555.5:p.Gly338=
ENST00000257555.10:c.1014C>A	ENSP00000257555.4:p.Gly338=
ENST00000400024.6:c.1014C>A	ENSP00000476181.1:p.Gly338=
ENST00000402929.5:n.1149C>A
ENST00000535955.5:n.43-1171C>A
ENST00000538626.2:n.191-1171C>A
ENST00000538646.5:c.827C>A	ENSP00000443964.1:p.Ala276Glu
ENST00000540108.1:c.*454C>A	ENSP00000445445.1:n.*454C>A
ENST00000541395.5:c.1014C>A	ENSP00000443112.1:p.Gly338=
ENST00000541924.5:c.*28C>A	ENSP00000440361.1:n.*28C>A
ENST00000543427.5:c.634-284C>A	ENSP00000439721.2:n.634-284C>A
ENST00000544413.2:c.1014C>A	ENSP00000438804.1:p.Gly338=
ENST00000544574.5:c.73-297C>A	ENSP00000438565.1:n.73-297C>A
ENST00000560968.5:c.894-63C>A
ENST00000615446.4:c.-199C>A	ENSP00000483994.1:n.-199C>A
ENST00000617366.4:c.587-1314C>A	ENSP00000481967.1:n.587-1314C>A
NM_000545.5:c.1014C>A , LRG_522t1:c.1014C>A	NP_000536.5:p.Gly338=
NM_000545.6:c.1014C>A	NP_000536.5:p.Gly338=
NM_001306179.1:c.1014C>A	NP_001293108.1:p.Gly338=
XM_005253931.2:c.1014C>A	XP_005253988.1:p.Gly338=
XM_024449168.1:c.1014C>A	XP_024304936.1:p.Gly338=
NM_000545.8:c.1014C>A MANE Select	NP_000536.6:p.Gly338=
NM_001306179.2:c.1014C>A	NP_001293108.2:p.Gly338=