Canonical Allele Identifier: CA2067685240
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997319_120997326delinsAGTGGCAG , CM000674.2:g.120997319_120997326delinsAGTGGCAG GRCh38
NC_000012.11:g.121435122_121435129delinsAGTGGCAG , CM000674.1:g.121435122_121435129delinsAGTGGCAG GRCh37
NC_000012.10:g.119919505_119919512delinsAGTGGCAG NCBI36
NG_011731.2:g.23574_23581delinsAGTGGCAG , LRG_522:g.23574_23581delinsAGTGGCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*57-155_*57-148delinsAGTGGCAG ENSP00000453965.2:n.*57-155_*57-148delinsAGTGGCAG
ENST00000257555.11:c.1310-155_1310-148delinsAGTGGCAG MANE Select ENSP00000257555.5:n.1310-155_1310-148delinsAGTGGCAG
ENST00000257555.10:c.1310-155_1310-148delinsAGTGGCAG ENSP00000257555.4:n.1310-155_1310-148delinsAGTGGCAG
ENST00000400024.6:c.1310-155_1310-148delinsAGTGGCAG ENSP00000476181.1:n.1310-155_1310-148delinsAGTGGCAG
ENST00000402929.5:n.2021_2028delinsAGTGGCAG
ENST00000535955.5:n.43-172_43-165delinsAGTGGCAG
ENST00000538626.2:n.191-172_191-165delinsAGTGGCAG
ENST00000538646.5:c.*286-155_*286-148delinsAGTGGCAG ENSP00000443964.1:n.*286-155_*286-148delinsAGTGGCAG
ENST00000540108.1:c.*750-155_*750-148delinsAGTGGCAG ENSP00000445445.1:n.*750-155_*750-148delinsAGTGGCAG
ENST00000541395.5:c.1310-155_1310-148delinsAGTGGCAG ENSP00000443112.1:n.1310-155_1310-148delinsAGTGGCAG
ENST00000541924.5:c.*324-155_*324-148delinsAGTGGCAG ENSP00000440361.1:n.*324-155_*324-148delinsAGTGGCAG
ENST00000543255.1:n.354-155_354-148delinsAGTGGCAG
ENST00000543427.5:c.773-155_773-148delinsAGTGGCAG ENSP00000439721.2:n.773-155_773-148delinsAGTGGCAG
ENST00000544413.2:c.1310-155_1310-148delinsAGTGGCAG ENSP00000438804.1:n.1310-155_1310-148delinsAGTGGCAG
ENST00000544574.5:c.*73-155_*73-148delinsAGTGGCAG ENSP00000438565.1:n.*73-155_*73-148delinsAGTGGCAG
ENST00000560968.5:c.1127-155_1127-148delinsAGTGGCAG
ENST00000615446.4:c.98-155_98-148delinsAGTGGCAG ENSP00000483994.1:n.98-155_98-148delinsAGTGGCAG
ENST00000617366.4:c.587-315_587-308delinsAGTGGCAG ENSP00000481967.1:n.587-315_587-308delinsAGTGGCAG
NM_000545.5:c.1310-155_1310-148delinsAGTGGCAG , LRG_522t1:c.1310-155_1310-148delinsAGTGGCAG NP_000536.5:n.1310-155_1310-148delinsAGTGGCAG
NM_000545.6:c.1310-155_1310-148delinsAGTGGCAG NP_000536.5:n.1310-155_1310-148delinsAGTGGCAG
NM_001306179.1:c.1310-155_1310-148delinsAGTGGCAG NP_001293108.1:n.1310-155_1310-148delinsAGTGGCAG
XM_005253931.2:c.1310-155_1310-148delinsAGTGGCAG XP_005253988.1:n.1310-155_1310-148delinsAGTGGCAG
XM_024449168.1:c.1310-155_1310-148delinsAGTGGCAG XP_024304936.1:n.1310-155_1310-148delinsAGTGGCAG
NM_000545.8:c.1310-155_1310-148delinsAGTGGCAG MANE Select NP_000536.6:n.1310-155_1310-148delinsAGTGGCAG
NM_001306179.2:c.1310-155_1310-148delinsAGTGGCAG NP_001293108.2:n.1310-155_1310-148delinsAGTGGCAG