Canonical Allele Identifier: CA386965035

Gene: HNF1A

Linked Data

• MyVariant Identifiers: chr12:g.121431473A>C (hg19) ; chr12:g.120993670A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120993670A>C , CM000674.2:g.120993670A>C	GRCh38
NC_000012.11:g.121431473A>C , CM000674.1:g.121431473A>C	GRCh37
NC_000012.10:g.119915856A>C	NCBI36
NG_011731.2:g.19925A>C , LRG_522:g.19925A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.677A>C	ENSP00000453965.2:p.Lys226Thr
ENST00000257555.11:c.677A>C MANE Select	ENSP00000257555.5:p.Lys226Thr
ENST00000257555.10:c.677A>C	ENSP00000257555.4:p.Lys226Thr
ENST00000400024.6:c.677A>C	ENSP00000476181.1:p.Lys226Thr
ENST00000402929.5:n.812A>C
ENST00000535955.5:n.43-3821A>C
ENST00000538626.2:n.191-3821A>C
ENST00000538646.5:c.527-494A>C	ENSP00000443964.1:n.527-494A>C
ENST00000540108.1:c.*117A>C	ENSP00000445445.1:n.*117A>C
ENST00000541395.5:c.677A>C	ENSP00000443112.1:p.Lys226Thr
ENST00000541924.5:c.677A>C	ENSP00000440361.1:p.Lys226Thr
ENST00000543427.5:c.633+44A>C	ENSP00000439721.2:n.633+44A>C
ENST00000544413.2:c.677A>C	ENSP00000438804.1:p.Lys226Thr
ENST00000544574.5:c.73-2947A>C	ENSP00000438565.1:n.73-2947A>C
ENST00000560968.5:c.820A>C
ENST00000615446.4:c.-257-2592A>C	ENSP00000483994.1:n.-257-2592A>C
ENST00000617366.4:c.586+91A>C	ENSP00000481967.1:n.586+91A>C
NM_000545.5:c.677A>C , LRG_522t1:c.677A>C	NP_000536.5:p.Lys226Thr
NM_000545.6:c.677A>C	NP_000536.5:p.Lys226Thr
NM_001306179.1:c.677A>C	NP_001293108.1:p.Lys226Thr
XM_005253931.2:c.677A>C	XP_005253988.1:p.Lys226Thr
XM_024449168.1:c.677A>C	XP_024304936.1:p.Lys226Thr
NM_000545.8:c.677A>C MANE Select	NP_000536.6:p.Lys226Thr
NM_001306179.2:c.677A>C	NP_001293108.2:p.Lys226Thr