Canonical Allele Identifier: CA645589504

Gene: HNF1A

Linked Data

• COSMIC: COSM1706376 ; COSM1706377

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120988918_120988919delinsAA , CM000674.2:g.120988918_120988919delinsAA	GRCh38
NC_000012.11:g.121426721_121426722delinsAA , CM000674.1:g.121426721_121426722delinsAA	GRCh37
NC_000012.10:g.119911104_119911105delinsAA	NCBI36
NG_011731.2:g.15173_15174delinsAA , LRG_522:g.15173_15174delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.412_413delinsAA	ENSP00000453965.2:p.Gly138Asn
ENST00000257555.11:c.412_413delinsAA MANE Select	ENSP00000257555.5:p.Gly138Asn
ENST00000257555.10:c.412_413delinsAA	ENSP00000257555.4:p.Gly138Asn
ENST00000400024.6:c.412_413delinsAA	ENSP00000476181.1:p.Gly138Asn
ENST00000402929.5:n.547_548delinsAA
ENST00000535955.5:n.43-8573_43-8572delinsAA
ENST00000538626.2:n.191-8573_191-8572delinsAA
ENST00000538646.5:c.412_413delinsAA	ENSP00000443964.1:p.Gly138Asn
ENST00000540108.1:c.327-4602_327-4601delinsAA	ENSP00000445445.1:n.327-4602_327-4601delinsAA
ENST00000541395.5:c.412_413delinsAA	ENSP00000443112.1:p.Gly138Asn
ENST00000541924.5:c.412_413delinsAA	ENSP00000440361.1:p.Gly138Asn
ENST00000543427.5:c.412_413delinsAA	ENSP00000439721.2:p.Gly138Asn
ENST00000544413.2:c.412_413delinsAA	ENSP00000438804.1:p.Gly138Asn
ENST00000544574.5:c.73-7699_73-7698delinsAA	ENSP00000438565.1:n.73-7699_73-7698delinsAA
ENST00000560968.5:c.555_556delinsAA
ENST00000615446.4:c.-257-7344_-257-7343delinsAA	ENSP00000483994.1:n.-257-7344_-257-7343delinsAA
ENST00000617366.4:c.412_413delinsAA	ENSP00000481967.1:p.Gly138Asn
NM_000545.5:c.412_413delinsAA , LRG_522t1:c.412_413delinsAA	NP_000536.5:p.Gly138Asn
NM_000545.6:c.412_413delinsAA	NP_000536.5:p.Gly138Asn
NM_001306179.1:c.412_413delinsAA	NP_001293108.1:p.Gly138Asn
XM_005253931.2:c.412_413delinsAA	XP_005253988.1:p.Gly138Asn
XM_024449168.1:c.412_413delinsAA	XP_024304936.1:p.Gly138Asn
NM_000545.8:c.412_413delinsAA MANE Select	NP_000536.6:p.Gly138Asn
NM_001306179.2:c.412_413delinsAA	NP_001293108.2:p.Gly138Asn