Canonical Allele Identifier: CA2621382406
Gene: HNF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120989073_120989074insTCCC , CM000674.2:g.120989073_120989074insTCCC GRCh38
NC_000012.11:g.121426876_121426877insTCCC , CM000674.1:g.121426876_121426877insTCCC GRCh37
NC_000012.10:g.119911259_119911260insTCCC NCBI36
NG_011731.2:g.15328_15329insTCCC , LRG_522:g.15328_15329insTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.526+41_526+42insTCCC ENSP00000453965.2:n.526+41_526+42insTCCC
ENST00000257555.11:c.526+41_526+42insTCCC MANE Select ENSP00000257555.5:n.526+41_526+42insTCCC
ENST00000257555.10:c.526+41_526+42insTCCC ENSP00000257555.4:n.526+41_526+42insTCCC
ENST00000400024.6:c.526+41_526+42insTCCC ENSP00000476181.1:n.526+41_526+42insTCCC
ENST00000402929.5:n.661+41_661+42insTCCC
ENST00000535955.5:n.43-8418_43-8417insTCCC
ENST00000538626.2:n.191-8418_191-8417insTCCC
ENST00000538646.5:c.526+41_526+42insTCCC ENSP00000443964.1:n.526+41_526+42insTCCC
ENST00000540108.1:c.327-4447_327-4446insTCCC ENSP00000445445.1:n.327-4447_327-4446insTCCC
ENST00000541395.5:c.526+41_526+42insTCCC ENSP00000443112.1:n.526+41_526+42insTCCC
ENST00000541924.5:c.526+41_526+42insTCCC ENSP00000440361.1:n.526+41_526+42insTCCC
ENST00000543427.5:c.526+41_526+42insTCCC ENSP00000439721.2:n.526+41_526+42insTCCC
ENST00000544413.2:c.526+41_526+42insTCCC ENSP00000438804.1:n.526+41_526+42insTCCC
ENST00000544574.5:c.73-7544_73-7543insTCCC ENSP00000438565.1:n.73-7544_73-7543insTCCC
ENST00000560968.5:c.669+41_669+42insTCCC
ENST00000615446.4:c.-257-7189_-257-7188insTCCC ENSP00000483994.1:n.-257-7189_-257-7188insTCCC
ENST00000617366.4:c.526+41_526+42insTCCC ENSP00000481967.1:n.526+41_526+42insTCCC
NM_000545.5:c.526+41_526+42insTCCC , LRG_522t1:c.526+41_526+42insTCCC NP_000536.5:n.526+41_526+42insTCCC
NM_000545.6:c.526+41_526+42insTCCC NP_000536.5:n.526+41_526+42insTCCC
NM_001306179.1:c.526+41_526+42insTCCC NP_001293108.1:n.526+41_526+42insTCCC
XM_005253931.2:c.526+41_526+42insTCCC XP_005253988.1:n.526+41_526+42insTCCC
XM_024449168.1:c.526+41_526+42insTCCC XP_024304936.1:n.526+41_526+42insTCCC
NM_000545.8:c.526+41_526+42insTCCC MANE Select NP_000536.6:n.526+41_526+42insTCCC
NM_001306179.2:c.526+41_526+42insTCCC NP_001293108.2:n.526+41_526+42insTCCC