Canonical Allele Identifier: CA6831682
Gene: HNF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 447485
dbSNP Id: rs377129682

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120978953A>G , CM000674.2:g.120978953A>G GRCh38
NC_000012.11:g.121416756A>G , CM000674.1:g.121416756A>G GRCh37
NC_000012.10:g.119901139A>G NCBI36
NG_011731.2:g.5208A>G , LRG_522:g.5208A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.185A>G ENSP00000453965.2:p.Asn62Ser
ENST00000257555.11:c.185A>G MANE Select ENSP00000257555.5:p.Asn62Ser
ENST00000257555.10:c.185A>G ENSP00000257555.4:p.Asn62Ser
ENST00000400024.6:c.185A>G ENSP00000476181.1:p.Asn62Ser
ENST00000402929.5:n.320A>G
ENST00000535955.5:n.42+261A>G
ENST00000538626.2:n.190+113A>G
ENST00000538646.5:c.185A>G ENSP00000443964.1:p.Asn62Ser
ENST00000540108.1:c.185A>G ENSP00000445445.1:p.Asn62Ser
ENST00000541395.5:c.185A>G ENSP00000443112.1:p.Asn62Ser
ENST00000541924.5:c.185A>G ENSP00000440361.1:p.Asn62Ser
ENST00000543427.5:c.185A>G ENSP00000439721.2:p.Asn62Ser
ENST00000544413.2:c.185A>G ENSP00000438804.1:p.Asn62Ser
ENST00000544574.5:c.72+113A>G ENSP00000438565.1:n.72+113A>G
ENST00000560968.5:c.328A>G
ENST00000615446.4:c.-258+242A>G ENSP00000483994.1:n.-258+242A>G
ENST00000617366.4:c.185A>G ENSP00000481967.1:p.Asn62Ser
NM_000545.5:c.185A>G , LRG_522t1:c.185A>G NP_000536.5:p.Asn62Ser
NM_000545.6:c.185A>G NP_000536.5:p.Asn62Ser
NM_001306179.1:c.185A>G NP_001293108.1:p.Asn62Ser
XM_005253931.2:c.185A>G XP_005253988.1:p.Asn62Ser
XM_024449168.1:c.185A>G XP_024304936.1:p.Asn62Ser
NM_000545.8:c.185A>G MANE Select NP_000536.6:p.Asn62Ser
NM_001306179.2:c.185A>G NP_001293108.2:p.Asn62Ser