Canonical Allele Identifier: CA2621383610
Gene: HNF1A HGNC NCBI

Linked Data

gnomAD v4: 12-120994131-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994131G>C , CM000674.2:g.120994131G>C GRCh38
NC_000012.11:g.121431934G>C , CM000674.1:g.121431934G>C GRCh37
NC_000012.10:g.119916317G>C NCBI36
NG_011731.2:g.20386G>C , LRG_522:g.20386G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.714-33G>C ENSP00000453965.2:n.714-33G>C
ENST00000257555.11:c.714-33G>C MANE Select ENSP00000257555.5:n.714-33G>C
ENST00000257555.10:c.714-33G>C ENSP00000257555.4:n.714-33G>C
ENST00000400024.6:c.714-33G>C ENSP00000476181.1:n.714-33G>C
ENST00000402929.5:n.849-33G>C
ENST00000535955.5:n.43-3360G>C
ENST00000538626.2:n.191-3360G>C
ENST00000538646.5:c.527-33G>C ENSP00000443964.1:n.527-33G>C
ENST00000540108.1:c.*154-33G>C ENSP00000445445.1:n.*154-33G>C
ENST00000541395.5:c.714-33G>C ENSP00000443112.1:n.714-33G>C
ENST00000541924.5:c.713+425G>C ENSP00000440361.1:n.713+425G>C
ENST00000543427.5:c.633+505G>C ENSP00000439721.2:n.633+505G>C
ENST00000544413.2:c.714-33G>C ENSP00000438804.1:n.714-33G>C
ENST00000544574.5:c.73-2486G>C ENSP00000438565.1:n.73-2486G>C
ENST00000560968.5:c.857-33G>C
ENST00000615446.4:c.-257-2131G>C ENSP00000483994.1:n.-257-2131G>C
ENST00000617366.4:c.586+552G>C ENSP00000481967.1:n.586+552G>C
NM_000545.5:c.714-33G>C , LRG_522t1:c.714-33G>C NP_000536.5:n.714-33G>C
NM_000545.6:c.714-33G>C NP_000536.5:n.714-33G>C
NM_001306179.1:c.714-33G>C NP_001293108.1:n.714-33G>C
XM_005253931.2:c.714-33G>C XP_005253988.1:n.714-33G>C
XM_024449168.1:c.714-33G>C XP_024304936.1:n.714-33G>C
NM_000545.8:c.714-33G>C MANE Select NP_000536.6:n.714-33G>C
NM_001306179.2:c.714-33G>C NP_001293108.2:n.714-33G>C
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