Canonical Allele Identifier: CA386966444
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs2135841991

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994280T>A , CM000674.2:g.120994280T>A GRCh38
NC_000012.11:g.121432083T>A , CM000674.1:g.121432083T>A GRCh37
NC_000012.10:g.119916466T>A NCBI36
NG_011731.2:g.20535T>A , LRG_522:g.20535T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+80T>A ENSP00000453965.2:n.750+80T>A
ENST00000257555.11:c.830T>A MANE Select ENSP00000257555.5:p.Phe277Tyr
ENST00000257555.10:c.830T>A ENSP00000257555.4:p.Phe277Tyr
ENST00000400024.6:c.830T>A ENSP00000476181.1:p.Phe277Tyr
ENST00000402929.5:n.965T>A
ENST00000535955.5:n.43-3211T>A
ENST00000538626.2:n.191-3211T>A
ENST00000538646.5:c.643T>A ENSP00000443964.1:p.Ser215Thr
ENST00000540108.1:c.*270T>A ENSP00000445445.1:n.*270T>A
ENST00000541395.5:c.830T>A ENSP00000443112.1:p.Phe277Tyr
ENST00000541924.5:c.713+574T>A ENSP00000440361.1:n.713+574T>A
ENST00000543427.5:c.633+654T>A ENSP00000439721.2:n.633+654T>A
ENST00000544413.2:c.830T>A ENSP00000438804.1:p.Phe277Tyr
ENST00000544574.5:c.73-2337T>A ENSP00000438565.1:n.73-2337T>A
ENST00000560968.5:c.893+80T>A
ENST00000615446.4:c.-257-1982T>A ENSP00000483994.1:n.-257-1982T>A
ENST00000617366.4:c.586+701T>A ENSP00000481967.1:n.586+701T>A
NM_000545.5:c.830T>A , LRG_522t1:c.830T>A NP_000536.5:p.Phe277Tyr
NM_000545.6:c.830T>A NP_000536.5:p.Phe277Tyr
NM_001306179.1:c.830T>A NP_001293108.1:p.Phe277Tyr
XM_005253931.2:c.830T>A XP_005253988.1:p.Phe277Tyr
XM_024449168.1:c.830T>A XP_024304936.1:p.Phe277Tyr
NM_000545.8:c.830T>A MANE Select NP_000536.6:p.Phe277Tyr
NM_001306179.2:c.830T>A NP_001293108.2:p.Phe277Tyr