Canonical Allele Identifier: CA2695217506

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120989027_120989037del , CM000674.2:g.120989027_120989037del	GRCh38
NC_000012.11:g.121426830_121426840del , CM000674.1:g.121426830_121426840del	GRCh37
NC_000012.10:g.119911213_119911223del	NCBI36
NG_011731.2:g.15282_15292del , LRG_522:g.15282_15292del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.521_526+5del
ENST00000257555.11:c.521_526+5del
ENST00000257555.10:c.521_526+5del
ENST00000400024.6:c.521_526+5del
ENST00000402929.5:n.656_661+5del
ENST00000535955.5:n.43-8464_43-8454del
ENST00000538626.2:n.191-8464_191-8454del
ENST00000538646.5:c.521_526+5del
ENST00000540108.1:c.327-4493_327-4483del	ENSP00000445445.1:n.327-4493_327-4483del
ENST00000541395.5:c.521_526+5del
ENST00000541924.5:c.521_526+5del
ENST00000543427.5:c.521_526+5del
ENST00000544413.2:c.521_526+5del
ENST00000544574.5:c.73-7590_73-7580del	ENSP00000438565.1:n.73-7590_73-7580del
ENST00000560968.5:c.664_669+5del
ENST00000615446.4:c.-257-7235_-257-7225del	ENSP00000483994.1:n.-257-7235_-257-7225del
ENST00000617366.4:c.521_526+5del
NM_000545.5:c.521_526+5del , LRG_522t1:c.521_526+5del
NM_000545.6:c.521_526+5del
NM_001306179.1:c.521_526+5del
XM_005253931.2:c.521_526+5del
XM_024449168.1:c.521_526+5del
NM_000545.8:c.521_526+5del
NM_001306179.2:c.521_526+5del