Canonical Allele Identifier: CA2067688659

Gene: HNF1A C12orf43

Linked Data

• dbSNP Id: rs1592901351

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121001546T>G , CM000674.2:g.121001546T>G	GRCh38
NC_000012.11:g.121439349T>G , CM000674.1:g.121439349T>G	GRCh37
NC_000012.10:g.119923732T>G	NCBI36
NG_011731.2:g.27801T>G , LRG_522:g.27801T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000560968.6:c.*997T>G (HNF1A)	ENSP00000453965.2:n.*997T>G
ENST00000257555.11:c.*354T>G (HNF1A) MANE Select	ENSP00000257555.5:n.*354T>G
ENST00000257555.10:c.*354T>G (HNF1A)	ENSP00000257555.4:n.*354T>G
ENST00000288757.7:c.*2607A>C (C12orf43) MANE Select	ENSP00000288757.5:n.*2607A>C
ENST00000540108.1:c.*1690T>G (HNF1A)	ENSP00000445445.1:n.*1690T>G
ENST00000541395.5:c.*354T>G (HNF1A)	ENSP00000443112.1:n.*354T>G
ENST00000543427.5:c.*354T>G (HNF1A)	ENSP00000439721.2:n.*354T>G
ENST00000560968.5:c.2067T>G (HNF1A)
ENST00000615446.4:c.*354T>G (HNF1A)	ENSP00000483994.1:n.*354T>G
ENST00000617366.4:c.*659T>G (HNF1A)	ENSP00000481967.1:n.*659T>G
NM_000545.5:c.*354T>G , LRG_522t1:c.*354T>G (HNF1A)	NP_000536.5:n.*354T>G
NM_000545.6:c.*354T>G (HNF1A)	NP_000536.5:n.*354T>G
NM_001306179.1:c.*354T>G (HNF1A)	NP_001293108.1:n.*354T>G
XM_005253931.2:c.*354T>G (HNF1A)	XP_005253988.1:n.*354T>G
XM_024449168.1:c.*354T>G (HNF1A)	XP_024304936.1:n.*354T>G
NM_000545.8:c.*354T>G (HNF1A) MANE Select	NP_000536.6:n.*354T>G
NM_001286191.2:c.*2607A>C (C12orf43)	NP_001273120.1:n.*2607A>C
NM_001286196.2:c.*2607A>C (C12orf43)	NP_001273125.1:n.*2607A>C
NM_001306179.2:c.*354T>G (HNF1A)	NP_001293108.2:n.*354T>G
NM_022895.3:c.*2607A>C (C12orf43) MANE Select	NP_075046.1:n.*2607A>C