Canonical Allele Identifier: CA2067678591
Gene: HNF1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993727C= , CM000674.2:g.120993727C= GRCh38
NC_000012.11:g.121431530C= , CM000674.1:g.121431530C= GRCh37
NC_000012.10:g.119915913C= NCBI36
NG_011731.2:g.19982C= , LRG_522:g.19982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.713+21C= ENSP00000453965.2:n.713+21C=
ENST00000257555.11:c.713+21C= MANE Select ENSP00000257555.5:n.713+21C=
ENST00000257555.10:c.713+21C= ENSP00000257555.4:n.713+21C=
ENST00000400024.6:c.713+21C= ENSP00000476181.1:n.713+21C=
ENST00000402929.5:n.848+21C=
ENST00000535955.5:n.43-3764C=
ENST00000538626.2:n.191-3764C=
ENST00000538646.5:c.527-437C= ENSP00000443964.1:n.527-437C=
ENST00000540108.1:c.*153+21C= ENSP00000445445.1:n.*153+21C=
ENST00000541395.5:c.713+21C= ENSP00000443112.1:n.713+21C=
ENST00000541924.5:c.713+21C= ENSP00000440361.1:n.713+21C=
ENST00000543427.5:c.633+101C= ENSP00000439721.2:n.633+101C=
ENST00000544413.2:c.713+21C= ENSP00000438804.1:n.713+21C=
ENST00000544574.5:c.73-2890C= ENSP00000438565.1:n.73-2890C=
ENST00000560968.5:c.856+21C=
ENST00000615446.4:c.-257-2535C= ENSP00000483994.1:n.-257-2535C=
ENST00000617366.4:c.586+148C= ENSP00000481967.1:n.586+148C=
NM_000545.5:c.713+21C= , LRG_522t1:c.713+21C= NP_000536.5:n.713+21C=
NM_000545.6:c.713+21C= NP_000536.5:n.713+21C=
NM_001306179.1:c.713+21C= NP_001293108.1:n.713+21C=
XM_005253931.2:c.713+21C= XP_005253988.1:n.713+21C=
XM_024449168.1:c.713+21C= XP_024304936.1:n.713+21C=
NM_000545.8:c.713+21C= MANE Select NP_000536.6:n.713+21C=
NM_001306179.2:c.713+21C= NP_001293108.2:n.713+21C=
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