Canonical Allele Identifier: CA2067673059

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120989118_120989120delinsTCC , CM000674.2:g.120989118_120989120delinsTCC	GRCh38
NC_000012.11:g.121426921_121426923delinsTCC , CM000674.1:g.121426921_121426923delinsTCC	GRCh37
NC_000012.10:g.119911304_119911306delinsTCC	NCBI36
NG_011731.2:g.15373_15375delinsTCC , LRG_522:g.15373_15375delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.526+86_526+88delinsTCC	ENSP00000453965.2:n.526+86_526+88delinsTCC
ENST00000257555.11:c.526+86_526+88delinsTCC MANE Select	ENSP00000257555.5:n.526+86_526+88delinsTCC
ENST00000257555.10:c.526+86_526+88delinsTCC	ENSP00000257555.4:n.526+86_526+88delinsTCC
ENST00000400024.6:c.526+86_526+88delinsTCC	ENSP00000476181.1:n.526+86_526+88delinsTCC
ENST00000402929.5:n.661+86_661+88delinsTCC
ENST00000535955.5:n.43-8373_43-8371delinsTCC
ENST00000538626.2:n.191-8373_191-8371delinsTCC
ENST00000538646.5:c.526+86_526+88delinsTCC	ENSP00000443964.1:n.526+86_526+88delinsTCC
ENST00000540108.1:c.327-4402_327-4400delinsTCC	ENSP00000445445.1:n.327-4402_327-4400delinsTCC
ENST00000541395.5:c.526+86_526+88delinsTCC	ENSP00000443112.1:n.526+86_526+88delinsTCC
ENST00000541924.5:c.526+86_526+88delinsTCC	ENSP00000440361.1:n.526+86_526+88delinsTCC
ENST00000543427.5:c.526+86_526+88delinsTCC	ENSP00000439721.2:n.526+86_526+88delinsTCC
ENST00000544413.2:c.526+86_526+88delinsTCC	ENSP00000438804.1:n.526+86_526+88delinsTCC
ENST00000544574.5:c.73-7499_73-7497delinsTCC	ENSP00000438565.1:n.73-7499_73-7497delinsTCC
ENST00000560968.5:c.669+86_669+88delinsTCC
ENST00000615446.4:c.-257-7144_-257-7142delinsTCC	ENSP00000483994.1:n.-257-7144_-257-7142delinsTCC
ENST00000617366.4:c.526+86_526+88delinsTCC	ENSP00000481967.1:n.526+86_526+88delinsTCC
NM_000545.5:c.526+86_526+88delinsTCC , LRG_522t1:c.526+86_526+88delinsTCC	NP_000536.5:n.526+86_526+88delinsTCC
NM_000545.6:c.526+86_526+88delinsTCC	NP_000536.5:n.526+86_526+88delinsTCC
NM_001306179.1:c.526+86_526+88delinsTCC	NP_001293108.1:n.526+86_526+88delinsTCC
XM_005253931.2:c.526+86_526+88delinsTCC	XP_005253988.1:n.526+86_526+88delinsTCC
XM_024449168.1:c.526+86_526+88delinsTCC	XP_024304936.1:n.526+86_526+88delinsTCC
NM_000545.8:c.526+86_526+88delinsTCC MANE Select	NP_000536.6:n.526+86_526+88delinsTCC
NM_001306179.2:c.526+86_526+88delinsTCC	NP_001293108.2:n.526+86_526+88delinsTCC