Canonical Allele Identifier: CA2067666417

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120982672_120982675delinsGTTA , CM000674.2:g.120982672_120982675delinsGTTA	GRCh38
NC_000012.11:g.121420475_121420478delinsGTTA , CM000674.1:g.121420475_121420478delinsGTTA	GRCh37
NC_000012.10:g.119904858_119904861delinsGTTA	NCBI36
NG_011731.2:g.8927_8930delinsGTTA , LRG_522:g.8927_8930delinsGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.326+3578_326+3581delinsGTTA	ENSP00000453965.2:n.326+3578_326+3581delinsGTTA
ENST00000257555.11:c.326+3578_326+3581delinsGTTA MANE Select	ENSP00000257555.5:n.326+3578_326+3581delinsGTTA
ENST00000257555.10:c.326+3578_326+3581delinsGTTA	ENSP00000257555.4:n.326+3578_326+3581delinsGTTA
ENST00000400024.6:c.326+3578_326+3581delinsGTTA	ENSP00000476181.1:n.326+3578_326+3581delinsGTTA
ENST00000402929.5:n.461+3578_461+3581delinsGTTA
ENST00000535955.5:n.42+3980_42+3983delinsGTTA
ENST00000538626.2:n.190+3832_190+3835delinsGTTA
ENST00000538646.5:c.326+3578_326+3581delinsGTTA	ENSP00000443964.1:n.326+3578_326+3581delinsGTTA
ENST00000540108.1:c.326+3578_326+3581delinsGTTA	ENSP00000445445.1:n.326+3578_326+3581delinsGTTA
ENST00000541395.5:c.326+3578_326+3581delinsGTTA	ENSP00000443112.1:n.326+3578_326+3581delinsGTTA
ENST00000541924.5:c.326+3578_326+3581delinsGTTA	ENSP00000440361.1:n.326+3578_326+3581delinsGTTA
ENST00000543427.5:c.326+3578_326+3581delinsGTTA	ENSP00000439721.2:n.326+3578_326+3581delinsGTTA
ENST00000544413.2:c.326+3578_326+3581delinsGTTA	ENSP00000438804.1:n.326+3578_326+3581delinsGTTA
ENST00000544574.5:c.72+3832_72+3835delinsGTTA	ENSP00000438565.1:n.72+3832_72+3835delinsGTTA
ENST00000560968.5:c.469+3578_469+3581delinsGTTA
ENST00000615446.4:c.-258+3961_-258+3964delinsGTTA	ENSP00000483994.1:n.-258+3961_-258+3964delinsGTTA
ENST00000617366.4:c.326+3578_326+3581delinsGTTA	ENSP00000481967.1:n.326+3578_326+3581delinsGTTA
NM_000545.5:c.326+3578_326+3581delinsGTTA , LRG_522t1:c.326+3578_326+3581delinsGTTA	NP_000536.5:n.326+3578_326+3581delinsGTTA
NM_000545.6:c.326+3578_326+3581delinsGTTA	NP_000536.5:n.326+3578_326+3581delinsGTTA
NM_001306179.1:c.326+3578_326+3581delinsGTTA	NP_001293108.1:n.326+3578_326+3581delinsGTTA
XM_005253931.2:c.326+3578_326+3581delinsGTTA	XP_005253988.1:n.326+3578_326+3581delinsGTTA
XM_024449168.1:c.326+3578_326+3581delinsGTTA	XP_024304936.1:n.326+3578_326+3581delinsGTTA
NM_000545.8:c.326+3578_326+3581delinsGTTA MANE Select	NP_000536.6:n.326+3578_326+3581delinsGTTA
NM_001306179.2:c.326+3578_326+3581delinsGTTA	NP_001293108.2:n.326+3578_326+3581delinsGTTA