Canonical Allele Identifier: CA2621390995
Gene: HNF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997358_120997362del , CM000674.2:g.120997358_120997362del GRCh38
NC_000012.11:g.121435161_121435165del , CM000674.1:g.121435161_121435165del GRCh37
NC_000012.10:g.119919544_119919548del NCBI36
NG_011731.2:g.23613_23617del , LRG_522:g.23613_23617del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*57-116_*57-112del ENSP00000453965.2:n.*57-116_*57-112del
ENST00000257555.11:c.1310-116_1310-112del MANE Select ENSP00000257555.5:n.1310-116_1310-112del
ENST00000257555.10:c.1310-116_1310-112del ENSP00000257555.4:n.1310-116_1310-112del
ENST00000400024.6:c.1310-116_1310-112del ENSP00000476181.1:n.1310-116_1310-112del
ENST00000402929.5:n.2060_2064del
ENST00000535955.5:n.43-133_43-129del
ENST00000538626.2:n.191-133_191-129del
ENST00000538646.5:c.*286-116_*286-112del ENSP00000443964.1:n.*286-116_*286-112del
ENST00000540108.1:c.*750-116_*750-112del ENSP00000445445.1:n.*750-116_*750-112del
ENST00000541395.5:c.1310-116_1310-112del ENSP00000443112.1:n.1310-116_1310-112del
ENST00000541924.5:c.*324-116_*324-112del ENSP00000440361.1:n.*324-116_*324-112del
ENST00000543255.1:n.354-116_354-112del
ENST00000543427.5:c.773-116_773-112del ENSP00000439721.2:n.773-116_773-112del
ENST00000544413.2:c.1310-116_1310-112del ENSP00000438804.1:n.1310-116_1310-112del
ENST00000544574.5:c.*73-116_*73-112del ENSP00000438565.1:n.*73-116_*73-112del
ENST00000560968.5:c.1127-116_1127-112del
ENST00000615446.4:c.98-116_98-112del ENSP00000483994.1:n.98-116_98-112del
ENST00000617366.4:c.587-276_587-272del ENSP00000481967.1:n.587-276_587-272del
NM_000545.5:c.1310-116_1310-112del , LRG_522t1:c.1310-116_1310-112del NP_000536.5:n.1310-116_1310-112del
NM_000545.6:c.1310-116_1310-112del NP_000536.5:n.1310-116_1310-112del
NM_001306179.1:c.1310-116_1310-112del NP_001293108.1:n.1310-116_1310-112del
XM_005253931.2:c.1310-116_1310-112del XP_005253988.1:n.1310-116_1310-112del
XM_024449168.1:c.1310-116_1310-112del XP_024304936.1:n.1310-116_1310-112del
NM_000545.8:c.1310-116_1310-112del MANE Select NP_000536.6:n.1310-116_1310-112del
NM_001306179.2:c.1310-116_1310-112del NP_001293108.2:n.1310-116_1310-112del