Canonical Allele Identifier: CA2067686000
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997585A= , CM000674.2:g.120997585A= GRCh38
NC_000012.11:g.121435388A= , CM000674.1:g.121435388A= GRCh37
NC_000012.10:g.119919771A= NCBI36
NG_011731.2:g.23840A= , LRG_522:g.23840A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*168A= ENSP00000453965.2:n.*168A=
ENST00000257555.11:c.1421A= MANE Select ENSP00000257555.5:p.Gln474=
ENST00000257555.10:c.1421A= ENSP00000257555.4:p.Gln474=
ENST00000400024.6:c.1421A= ENSP00000476181.1:p.Gln474=
ENST00000402929.5:n.2287A=
ENST00000535955.5:n.137A=
ENST00000538626.2:n.285A=
ENST00000538646.5:c.*397A= ENSP00000443964.1:n.*397A=
ENST00000540108.1:c.*861A= ENSP00000445445.1:n.*861A=
ENST00000541395.5:c.1421A= ENSP00000443112.1:p.Gln474=
ENST00000541924.5:c.*435A= ENSP00000440361.1:n.*435A=
ENST00000543255.1:n.465A=
ENST00000543427.5:c.884A= ENSP00000439721.2:p.Gln295=
ENST00000544413.2:c.1421A= ENSP00000438804.1:p.Gln474=
ENST00000544574.5:c.*184A= ENSP00000438565.1:n.*184A=
ENST00000560968.5:c.1238A=
ENST00000615446.4:c.209A= ENSP00000483994.1:p.Gln70=
ENST00000617366.4:c.587-49A= ENSP00000481967.1:n.587-49A=
NM_000545.5:c.1421A= , LRG_522t1:c.1421A= NP_000536.5:p.Gln474=
NM_000545.6:c.1421A= NP_000536.5:p.Gln474=
NM_001306179.1:c.1421A= NP_001293108.1:p.Gln474=
XM_005253931.2:c.1421A= XP_005253988.1:p.Gln474=
XM_024449168.1:c.1421A= XP_024304936.1:p.Gln474=
NM_000545.8:c.1421A= MANE Select NP_000536.6:p.Gln474=
NM_001306179.2:c.1421A= NP_001293108.2:p.Gln474=