Canonical Allele Identifier: CA645589506

Gene: HNF1A

Linked Data

• COSMIC: COSM24913 ; COSM3666554 ; COSM3666555

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120989033_120989045del , CM000674.2:g.120989033_120989045del	GRCh38
NC_000012.11:g.121426836_121426848del , CM000674.1:g.121426836_121426848del	GRCh37
NC_000012.10:g.119911219_119911231del	NCBI36
NG_011731.2:g.15288_15300del , LRG_522:g.15288_15300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.526+1_526+13del
ENST00000257555.11:c.526+1_526+13del
ENST00000257555.10:c.526+1_526+13del
ENST00000400024.6:c.526+1_526+13del
ENST00000402929.5:n.661+1_661+13del
ENST00000535955.5:n.43-8458_43-8446del
ENST00000538626.2:n.191-8458_191-8446del
ENST00000538646.5:c.526+1_526+13del
ENST00000540108.1:c.327-4487_327-4475del	ENSP00000445445.1:n.327-4487_327-4475del
ENST00000541395.5:c.526+1_526+13del
ENST00000541924.5:c.526+1_526+13del
ENST00000543427.5:c.526+1_526+13del
ENST00000544413.2:c.526+1_526+13del
ENST00000544574.5:c.73-7584_73-7572del	ENSP00000438565.1:n.73-7584_73-7572del
ENST00000560968.5:c.669+1_669+13del
ENST00000615446.4:c.-257-7229_-257-7217del	ENSP00000483994.1:n.-257-7229_-257-7217del
ENST00000617366.4:c.526+1_526+13del
NM_000545.5:c.526+1_526+13del , LRG_522t1:c.526+1_526+13del
NM_000545.6:c.526+1_526+13del
NM_001306179.1:c.526+1_526+13del
XM_005253931.2:c.526+1_526+13del
XM_024449168.1:c.526+1_526+13del
NM_000545.8:c.526+1_526+13del
NM_001306179.2:c.526+1_526+13del