Canonical Allele Identifier: CA386970123

Gene: HNF1A

Linked Data

• gnomAD v4: 12-120997544-G-T
• MyVariant Identifiers: chr12:g.121435347G>T (hg19) ; chr12:g.120997544G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120997544G>T , CM000674.2:g.120997544G>T	GRCh38
NC_000012.11:g.121435347G>T , CM000674.1:g.121435347G>T	GRCh37
NC_000012.10:g.119919730G>T	NCBI36
NG_011731.2:g.23799G>T , LRG_522:g.23799G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.*127G>T	ENSP00000453965.2:n.*127G>T
ENST00000257555.11:c.1380G>T MANE Select	ENSP00000257555.5:p.Gln460His
ENST00000257555.10:c.1380G>T	ENSP00000257555.4:p.Gln460His
ENST00000400024.6:c.1380G>T	ENSP00000476181.1:p.Gln460His
ENST00000402929.5:n.2246G>T
ENST00000535955.5:n.96G>T
ENST00000538626.2:n.244G>T
ENST00000538646.5:c.*356G>T	ENSP00000443964.1:n.*356G>T
ENST00000540108.1:c.*820G>T	ENSP00000445445.1:n.*820G>T
ENST00000541395.5:c.1380G>T	ENSP00000443112.1:p.Gln460His
ENST00000541924.5:c.*394G>T	ENSP00000440361.1:n.*394G>T
ENST00000543255.1:n.424G>T
ENST00000543427.5:c.843G>T	ENSP00000439721.2:p.Gln281His
ENST00000544413.2:c.1380G>T	ENSP00000438804.1:p.Gln460His
ENST00000544574.5:c.*143G>T	ENSP00000438565.1:n.*143G>T
ENST00000560968.5:c.1197G>T
ENST00000615446.4:c.168G>T	ENSP00000483994.1:p.Gln56His
ENST00000617366.4:c.587-90G>T	ENSP00000481967.1:n.587-90G>T
NM_000545.5:c.1380G>T , LRG_522t1:c.1380G>T	NP_000536.5:p.Gln460His
NM_000545.6:c.1380G>T	NP_000536.5:p.Gln460His
NM_001306179.1:c.1380G>T	NP_001293108.1:p.Gln460His
XM_005253931.2:c.1380G>T	XP_005253988.1:p.Gln460His
XM_024449168.1:c.1380G>T	XP_024304936.1:p.Gln460His
NM_000545.8:c.1380G>T MANE Select	NP_000536.6:p.Gln460His
NM_001306179.2:c.1380G>T	NP_001293108.2:p.Gln460His