Canonical Allele Identifier: CA386967880

Gene: HNF1A

Linked Data

• MyVariant Identifiers: chr12:g.121434077G>T (hg19) ; chr12:g.120996274G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996274G>T , CM000674.2:g.120996274G>T	GRCh38
NC_000012.11:g.121434077G>T , CM000674.1:g.121434077G>T	GRCh37
NC_000012.10:g.119918460G>T	NCBI36
NG_011731.2:g.22529G>T , LRG_522:g.22529G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.751-109G>T	ENSP00000453965.2:n.751-109G>T
ENST00000257555.11:c.968G>T MANE Select	ENSP00000257555.5:p.Gly323Val
ENST00000257555.10:c.968G>T	ENSP00000257555.4:p.Gly323Val
ENST00000400024.6:c.968G>T	ENSP00000476181.1:p.Gly323Val
ENST00000402929.5:n.1103G>T
ENST00000535955.5:n.43-1217G>T
ENST00000538626.2:n.191-1217G>T
ENST00000538646.5:c.781G>T	ENSP00000443964.1:p.Asp261Tyr
ENST00000540108.1:c.*408G>T	ENSP00000445445.1:n.*408G>T
ENST00000541395.5:c.968G>T	ENSP00000443112.1:p.Gly323Val
ENST00000541924.5:c.726G>T	ENSP00000440361.1:p.Trp242Cys
ENST00000543427.5:c.634-330G>T	ENSP00000439721.2:n.634-330G>T
ENST00000544413.2:c.968G>T	ENSP00000438804.1:p.Gly323Val
ENST00000544574.5:c.73-343G>T	ENSP00000438565.1:n.73-343G>T
ENST00000560968.5:c.894-109G>T
ENST00000615446.4:c.-245G>T	ENSP00000483994.1:n.-245G>T
ENST00000617366.4:c.587-1360G>T	ENSP00000481967.1:n.587-1360G>T
NM_000545.5:c.968G>T , LRG_522t1:c.968G>T	NP_000536.5:p.Gly323Val
NM_000545.6:c.968G>T	NP_000536.5:p.Gly323Val
NM_001306179.1:c.968G>T	NP_001293108.1:p.Gly323Val
XM_005253931.2:c.968G>T	XP_005253988.1:p.Gly323Val
XM_024449168.1:c.968G>T	XP_024304936.1:p.Gly323Val
NM_000545.8:c.968G>T MANE Select	NP_000536.6:p.Gly323Val
NM_001306179.2:c.968G>T	NP_001293108.2:p.Gly323Val