Canonical Allele Identifier: CA386954869
Gene: HNF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1327593
ClinVar RCV Id: RCV001794537
dbSNP Id: rs2135820404
MyVariant Identifiers: chr12:g.121416890C>A (hg19) chr12:g.120979087C>A (hg38)
ERepo: CA386954869/MONDO:0015967/017
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120979087C>A , CM000674.2:g.120979087C>A GRCh38
NC_000012.11:g.121416890C>A , CM000674.1:g.121416890C>A GRCh37
NC_000012.10:g.119901273C>A NCBI36
NG_011731.2:g.5342C>A , LRG_522:g.5342C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000560968.6:c.319C>A ENSP00000453965.2:p.Leu107Ile
ENST00000257555.11:c.319C>A MANE Select ENSP00000257555.5:p.Leu107Ile
ENST00000257555.10:c.319C>A ENSP00000257555.4:p.Leu107Ile
ENST00000400024.6:c.319C>A ENSP00000476181.1:p.Leu107Ile
ENST00000402929.5:n.454C>A
ENST00000535955.5:n.42+395C>A
ENST00000538626.2:n.190+247C>A
ENST00000538646.5:c.319C>A ENSP00000443964.1:p.Leu107Ile
ENST00000540108.1:c.319C>A ENSP00000445445.1:p.Leu107Ile
ENST00000541395.5:c.319C>A ENSP00000443112.1:p.Leu107Ile
ENST00000541924.5:c.319C>A ENSP00000440361.1:p.Leu107Ile
ENST00000543427.5:c.319C>A ENSP00000439721.2:p.Leu107Ile
ENST00000544413.2:c.319C>A ENSP00000438804.1:p.Leu107Ile
ENST00000544574.5:c.72+247C>A ENSP00000438565.1:n.72+247C>A
ENST00000560968.5:c.462C>A
ENST00000615446.4:c.-258+376C>A ENSP00000483994.1:n.-258+376C>A
ENST00000617366.4:c.319C>A ENSP00000481967.1:p.Leu107Ile
NM_000545.5:c.319C>A , LRG_522t1:c.319C>A NP_000536.5:p.Leu107Ile
NM_000545.6:c.319C>A NP_000536.5:p.Leu107Ile
NM_001306179.1:c.319C>A NP_001293108.1:p.Leu107Ile
XM_005253931.2:c.319C>A XP_005253988.1:p.Leu107Ile
XM_024449168.1:c.319C>A XP_024304936.1:p.Leu107Ile
NM_000545.8:c.319C>A MANE Select NP_000536.6:p.Leu107Ile
NM_001306179.2:c.319C>A NP_001293108.2:p.Leu107Ile
Search 100 bp 5'
Search 100 bp 3'