Canonical Allele Identifier: CA386963811

Gene: HNF1A

Linked Data

• dbSNP Id: rs2135839025
• MyVariant Identifiers: chr12:g.121431365C>G (hg19) ; chr12:g.120993562C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120993562C>G , CM000674.2:g.120993562C>G	GRCh38
NC_000012.11:g.121431365C>G , CM000674.1:g.121431365C>G	GRCh37
NC_000012.10:g.119915748C>G	NCBI36
NG_011731.2:g.19817C>G , LRG_522:g.19817C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000560968.6:c.569C>G	ENSP00000453965.2:p.Thr190Arg
ENST00000257555.11:c.569C>G MANE Select	ENSP00000257555.5:p.Thr190Arg
ENST00000257555.10:c.569C>G	ENSP00000257555.4:p.Thr190Arg
ENST00000400024.6:c.569C>G	ENSP00000476181.1:p.Thr190Arg
ENST00000402929.5:n.704C>G
ENST00000535955.5:n.43-3929C>G
ENST00000538626.2:n.191-3929C>G
ENST00000538646.5:c.527-602C>G	ENSP00000443964.1:n.527-602C>G
ENST00000540108.1:c.*9C>G	ENSP00000445445.1:n.*9C>G
ENST00000541395.5:c.569C>G	ENSP00000443112.1:p.Thr190Arg
ENST00000541924.5:c.569C>G	ENSP00000440361.1:p.Thr190Arg
ENST00000543427.5:c.569C>G	ENSP00000439721.2:p.Thr190Arg
ENST00000544413.2:c.569C>G	ENSP00000438804.1:p.Thr190Arg
ENST00000544574.5:c.73-3055C>G	ENSP00000438565.1:n.73-3055C>G
ENST00000560968.5:c.712C>G
ENST00000615446.4:c.-257-2700C>G	ENSP00000483994.1:n.-257-2700C>G
ENST00000617366.4:c.569C>G	ENSP00000481967.1:p.Thr190Arg
NM_000545.5:c.569C>G , LRG_522t1:c.569C>G	NP_000536.5:p.Thr190Arg
NM_000545.6:c.569C>G	NP_000536.5:p.Thr190Arg
NM_001306179.1:c.569C>G	NP_001293108.1:p.Thr190Arg
XM_005253931.2:c.569C>G	XP_005253988.1:p.Thr190Arg
XM_024449168.1:c.569C>G	XP_024304936.1:p.Thr190Arg
NM_000545.8:c.569C>G MANE Select	NP_000536.6:p.Thr190Arg
NM_001306179.2:c.569C>G	NP_001293108.2:p.Thr190Arg