Canonical Allele Identifier: CA2067673091
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120989189_120989190delinsGC , CM000674.2:g.120989189_120989190delinsGC GRCh38
NC_000012.11:g.121426992_121426993delinsGC , CM000674.1:g.121426992_121426993delinsGC GRCh37
NC_000012.10:g.119911375_119911376delinsGC NCBI36
NG_011731.2:g.15444_15445delinsGC , LRG_522:g.15444_15445delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.526+157_526+158delinsGC ENSP00000453965.2:n.526+157_526+158delinsGC
ENST00000257555.11:c.526+157_526+158delinsGC MANE Select ENSP00000257555.5:n.526+157_526+158delinsGC
ENST00000257555.10:c.526+157_526+158delinsGC ENSP00000257555.4:n.526+157_526+158delinsGC
ENST00000400024.6:c.526+157_526+158delinsGC ENSP00000476181.1:n.526+157_526+158delinsGC
ENST00000402929.5:n.661+157_661+158delinsGC
ENST00000535955.5:n.43-8302_43-8301delinsGC
ENST00000538626.2:n.191-8302_191-8301delinsGC
ENST00000538646.5:c.526+157_526+158delinsGC ENSP00000443964.1:n.526+157_526+158delinsGC
ENST00000540108.1:c.327-4331_327-4330delinsGC ENSP00000445445.1:n.327-4331_327-4330delinsGC
ENST00000541395.5:c.526+157_526+158delinsGC ENSP00000443112.1:n.526+157_526+158delinsGC
ENST00000541924.5:c.526+157_526+158delinsGC ENSP00000440361.1:n.526+157_526+158delinsGC
ENST00000543427.5:c.526+157_526+158delinsGC ENSP00000439721.2:n.526+157_526+158delinsGC
ENST00000544413.2:c.526+157_526+158delinsGC ENSP00000438804.1:n.526+157_526+158delinsGC
ENST00000544574.5:c.73-7428_73-7427delinsGC ENSP00000438565.1:n.73-7428_73-7427delinsGC
ENST00000560968.5:c.669+157_669+158delinsGC
ENST00000615446.4:c.-257-7073_-257-7072delinsGC ENSP00000483994.1:n.-257-7073_-257-7072delinsGC
ENST00000617366.4:c.526+157_526+158delinsGC ENSP00000481967.1:n.526+157_526+158delinsGC
NM_000545.5:c.526+157_526+158delinsGC , LRG_522t1:c.526+157_526+158delinsGC NP_000536.5:n.526+157_526+158delinsGC
NM_000545.6:c.526+157_526+158delinsGC NP_000536.5:n.526+157_526+158delinsGC
NM_001306179.1:c.526+157_526+158delinsGC NP_001293108.1:n.526+157_526+158delinsGC
XM_005253931.2:c.526+157_526+158delinsGC XP_005253988.1:n.526+157_526+158delinsGC
XM_024449168.1:c.526+157_526+158delinsGC XP_024304936.1:n.526+157_526+158delinsGC
NM_000545.8:c.526+157_526+158delinsGC MANE Select NP_000536.6:n.526+157_526+158delinsGC
NM_001306179.2:c.526+157_526+158delinsGC NP_001293108.2:n.526+157_526+158delinsGC