Canonical Allele Identifier: CA386970100

Gene: HNF1A

Linked Data

• dbSNP Id: rs2135847598
• MyVariant Identifiers: chr12:g.121435336A>G (hg19) ; chr12:g.120997533A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120997533A>G , CM000674.2:g.120997533A>G	GRCh38
NC_000012.11:g.121435336A>G , CM000674.1:g.121435336A>G	GRCh37
NC_000012.10:g.119919719A>G	NCBI36
NG_011731.2:g.23788A>G , LRG_522:g.23788A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.*116A>G	ENSP00000453965.2:n.*116A>G
ENST00000257555.11:c.1369A>G MANE Select	ENSP00000257555.5:p.Thr457Ala
ENST00000257555.10:c.1369A>G	ENSP00000257555.4:p.Thr457Ala
ENST00000400024.6:c.1369A>G	ENSP00000476181.1:p.Thr457Ala
ENST00000402929.5:n.2235A>G
ENST00000535955.5:n.85A>G
ENST00000538626.2:n.233A>G
ENST00000538646.5:c.*345A>G	ENSP00000443964.1:n.*345A>G
ENST00000540108.1:c.*809A>G	ENSP00000445445.1:n.*809A>G
ENST00000541395.5:c.1369A>G	ENSP00000443112.1:p.Thr457Ala
ENST00000541924.5:c.*383A>G	ENSP00000440361.1:n.*383A>G
ENST00000543255.1:n.413A>G
ENST00000543427.5:c.832A>G	ENSP00000439721.2:p.Thr278Ala
ENST00000544413.2:c.1369A>G	ENSP00000438804.1:p.Thr457Ala
ENST00000544574.5:c.*132A>G	ENSP00000438565.1:n.*132A>G
ENST00000560968.5:c.1186A>G
ENST00000615446.4:c.157A>G	ENSP00000483994.1:p.Thr53Ala
ENST00000617366.4:c.587-101A>G	ENSP00000481967.1:n.587-101A>G
NM_000545.5:c.1369A>G , LRG_522t1:c.1369A>G	NP_000536.5:p.Thr457Ala
NM_000545.6:c.1369A>G	NP_000536.5:p.Thr457Ala
NM_001306179.1:c.1369A>G	NP_001293108.1:p.Thr457Ala
XM_005253931.2:c.1369A>G	XP_005253988.1:p.Thr457Ala
XM_024449168.1:c.1369A>G	XP_024304936.1:p.Thr457Ala
NM_000545.8:c.1369A>G MANE Select	NP_000536.6:p.Thr457Ala
NM_001306179.2:c.1369A>G	NP_001293108.2:p.Thr457Ala