Canonical Allele Identifier: CA2621390962
Gene: HNF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997336_120997337insTGGTC , CM000674.2:g.120997336_120997337insTGGTC GRCh38
NC_000012.11:g.121435139_121435140insTGGTC , CM000674.1:g.121435139_121435140insTGGTC GRCh37
NC_000012.10:g.119919522_119919523insTGGTC NCBI36
NG_011731.2:g.23591_23592insTGGTC , LRG_522:g.23591_23592insTGGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*57-138_*57-137insTGGTC ENSP00000453965.2:n.*57-138_*57-137insTGGTC
ENST00000257555.11:c.1310-138_1310-137insTGGTC MANE Select ENSP00000257555.5:n.1310-138_1310-137insTGGTC
ENST00000257555.10:c.1310-138_1310-137insTGGTC ENSP00000257555.4:n.1310-138_1310-137insTGGTC
ENST00000400024.6:c.1310-138_1310-137insTGGTC ENSP00000476181.1:n.1310-138_1310-137insTGGTC
ENST00000402929.5:n.2038_2039insTGGTC
ENST00000535955.5:n.43-155_43-154insTGGTC
ENST00000538626.2:n.191-155_191-154insTGGTC
ENST00000538646.5:c.*286-138_*286-137insTGGTC ENSP00000443964.1:n.*286-138_*286-137insTGGTC
ENST00000540108.1:c.*750-138_*750-137insTGGTC ENSP00000445445.1:n.*750-138_*750-137insTGGTC
ENST00000541395.5:c.1310-138_1310-137insTGGTC ENSP00000443112.1:n.1310-138_1310-137insTGGTC
ENST00000541924.5:c.*324-138_*324-137insTGGTC ENSP00000440361.1:n.*324-138_*324-137insTGGTC
ENST00000543255.1:n.354-138_354-137insTGGTC
ENST00000543427.5:c.773-138_773-137insTGGTC ENSP00000439721.2:n.773-138_773-137insTGGTC
ENST00000544413.2:c.1310-138_1310-137insTGGTC ENSP00000438804.1:n.1310-138_1310-137insTGGTC
ENST00000544574.5:c.*73-138_*73-137insTGGTC ENSP00000438565.1:n.*73-138_*73-137insTGGTC
ENST00000560968.5:c.1127-138_1127-137insTGGTC
ENST00000615446.4:c.98-138_98-137insTGGTC ENSP00000483994.1:n.98-138_98-137insTGGTC
ENST00000617366.4:c.587-298_587-297insTGGTC ENSP00000481967.1:n.587-298_587-297insTGGTC
NM_000545.5:c.1310-138_1310-137insTGGTC , LRG_522t1:c.1310-138_1310-137insTGGTC NP_000536.5:n.1310-138_1310-137insTGGTC
NM_000545.6:c.1310-138_1310-137insTGGTC NP_000536.5:n.1310-138_1310-137insTGGTC
NM_001306179.1:c.1310-138_1310-137insTGGTC NP_001293108.1:n.1310-138_1310-137insTGGTC
XM_005253931.2:c.1310-138_1310-137insTGGTC XP_005253988.1:n.1310-138_1310-137insTGGTC
XM_024449168.1:c.1310-138_1310-137insTGGTC XP_024304936.1:n.1310-138_1310-137insTGGTC
NM_000545.8:c.1310-138_1310-137insTGGTC MANE Select NP_000536.6:n.1310-138_1310-137insTGGTC
NM_001306179.2:c.1310-138_1310-137insTGGTC NP_001293108.2:n.1310-138_1310-137insTGGTC