Canonical Allele Identifier: CA482163999

Gene: HNF1A

Linked Data

• MyVariant Identifiers: chr12:g.121431366A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120993563A>T , CM000674.2:g.120993563A>T	GRCh38
NC_000012.11:g.121431366A>T , CM000674.1:g.121431366A>T	GRCh37
NC_000012.10:g.119915749A>T	NCBI36
NG_011731.2:g.19818A>T , LRG_522:g.19818A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000560968.6:c.570A>T	ENSP00000453965.2:p.Thr190=
ENST00000257555.11:c.570A>T MANE Select	ENSP00000257555.5:p.Thr190=
ENST00000257555.10:c.570A>T	ENSP00000257555.4:p.Thr190=
ENST00000400024.6:c.570A>T	ENSP00000476181.1:p.Thr190=
ENST00000402929.5:n.705A>T
ENST00000535955.5:n.43-3928A>T
ENST00000538626.2:n.191-3928A>T
ENST00000538646.5:c.527-601A>T	ENSP00000443964.1:n.527-601A>T
ENST00000540108.1:c.*10A>T	ENSP00000445445.1:n.*10A>T
ENST00000541395.5:c.570A>T	ENSP00000443112.1:p.Thr190=
ENST00000541924.5:c.570A>T	ENSP00000440361.1:p.Thr190=
ENST00000543427.5:c.570A>T	ENSP00000439721.2:p.Thr190=
ENST00000544413.2:c.570A>T	ENSP00000438804.1:p.Thr190=
ENST00000544574.5:c.73-3054A>T	ENSP00000438565.1:n.73-3054A>T
ENST00000560968.5:c.713A>T
ENST00000615446.4:c.-257-2699A>T	ENSP00000483994.1:n.-257-2699A>T
ENST00000617366.4:c.570A>T	ENSP00000481967.1:p.Thr190=
NM_000545.5:c.570A>T , LRG_522t1:c.570A>T	NP_000536.5:p.Thr190=
NM_000545.6:c.570A>T	NP_000536.5:p.Thr190=
NM_001306179.1:c.570A>T	NP_001293108.1:p.Thr190=
XM_005253931.2:c.570A>T	XP_005253988.1:p.Thr190=
XM_024449168.1:c.570A>T	XP_024304936.1:p.Thr190=
NM_000545.8:c.570A>T MANE Select	NP_000536.6:p.Thr190=
NM_001306179.2:c.570A>T	NP_001293108.2:p.Thr190=