Canonical Allele Identifier: CA386968718

Gene: HNF1A

Linked Data

• dbSNP Id: rs2135845451
• MyVariant Identifiers: chr12:g.121434218T>A (hg19) ; chr12:g.120996415T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996415T>A , CM000674.2:g.120996415T>A	GRCh38
NC_000012.11:g.121434218T>A , CM000674.1:g.121434218T>A	GRCh37
NC_000012.10:g.119918601T>A	NCBI36
NG_011731.2:g.22670T>A , LRG_522:g.22670T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.781+2T>A	ENSP00000453965.2:n.781+2T>A
ENST00000257555.11:c.1107+2T>A MANE Select	ENSP00000257555.5:n.1107+2T>A
ENST00000257555.10:c.1107+2T>A	ENSP00000257555.4:n.1107+2T>A
ENST00000400024.6:c.1107+2T>A	ENSP00000476181.1:n.1107+2T>A
ENST00000402929.5:n.1242+2T>A
ENST00000535955.5:n.43-1076T>A
ENST00000538626.2:n.191-1076T>A
ENST00000538646.5:c.*83+2T>A	ENSP00000443964.1:n.*83+2T>A
ENST00000540108.1:c.*547+2T>A	ENSP00000445445.1:n.*547+2T>A
ENST00000541395.5:c.1107+2T>A	ENSP00000443112.1:n.1107+2T>A
ENST00000541924.5:c.*121+2T>A	ENSP00000440361.1:n.*121+2T>A
ENST00000543255.1:n.26T>A
ENST00000543427.5:c.634-189T>A	ENSP00000439721.2:n.634-189T>A
ENST00000544413.2:c.1107+2T>A	ENSP00000438804.1:n.1107+2T>A
ENST00000544574.5:c.73-202T>A	ENSP00000438565.1:n.73-202T>A
ENST00000560968.5:c.924+2T>A
ENST00000615446.4:c.-106+2T>A	ENSP00000483994.1:n.-106+2T>A
ENST00000617366.4:c.587-1219T>A	ENSP00000481967.1:n.587-1219T>A
NM_000545.5:c.1107+2T>A , LRG_522t1:c.1107+2T>A	NP_000536.5:n.1107+2T>A
NM_000545.6:c.1107+2T>A	NP_000536.5:n.1107+2T>A
NM_001306179.1:c.1107+2T>A	NP_001293108.1:n.1107+2T>A
XM_005253931.2:c.1107+2T>A	XP_005253988.1:n.1107+2T>A
XM_024449168.1:c.1107+2T>A	XP_024304936.1:n.1107+2T>A
NM_000545.8:c.1107+2T>A MANE Select	NP_000536.6:n.1107+2T>A
NM_001306179.2:c.1107+2T>A	NP_001293108.2:n.1107+2T>A