Canonical Allele Identifier: CA386970331

Gene: HNF1A

Linked Data

• dbSNP Id: rs2135848103
• MyVariant Identifiers: chr12:g.121435439C>T (hg19) ; chr12:g.120997636C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120997636C>T , CM000674.2:g.120997636C>T	GRCh38
NC_000012.11:g.121435439C>T , CM000674.1:g.121435439C>T	GRCh37
NC_000012.10:g.119919822C>T	NCBI36
NG_011731.2:g.23891C>T , LRG_522:g.23891C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000560968.6:c.*219C>T	ENSP00000453965.2:n.*219C>T
ENST00000257555.11:c.1472C>T MANE Select	ENSP00000257555.5:p.Ala491Val
ENST00000257555.10:c.1472C>T	ENSP00000257555.4:p.Ala491Val
ENST00000400024.6:c.1472C>T	ENSP00000476181.1:p.Ala491Val
ENST00000402929.5:n.2338C>T
ENST00000535955.5:n.188C>T
ENST00000538626.2:n.336C>T
ENST00000538646.5:c.*448C>T	ENSP00000443964.1:n.*448C>T
ENST00000540108.1:c.*912C>T	ENSP00000445445.1:n.*912C>T
ENST00000541395.5:c.1472C>T	ENSP00000443112.1:p.Ala491Val
ENST00000541924.5:c.*486C>T	ENSP00000440361.1:n.*486C>T
ENST00000543255.1:n.516C>T
ENST00000543427.5:c.935C>T	ENSP00000439721.2:p.Ala312Val
ENST00000544413.2:c.1472C>T	ENSP00000438804.1:p.Ala491Val
ENST00000544574.5:c.*235C>T	ENSP00000438565.1:n.*235C>T
ENST00000560968.5:c.1289C>T
ENST00000615446.4:c.260C>T	ENSP00000483994.1:p.Ala87Val
ENST00000617366.4:c.589C>T	ENSP00000481967.1:p.Pro197Ser
NM_000545.5:c.1472C>T , LRG_522t1:c.1472C>T	NP_000536.5:p.Ala491Val
NM_000545.6:c.1472C>T	NP_000536.5:p.Ala491Val
NM_001306179.1:c.1472C>T	NP_001293108.1:p.Ala491Val
XM_005253931.2:c.1472C>T	XP_005253988.1:p.Ala491Val
XM_024449168.1:c.1472C>T	XP_024304936.1:p.Ala491Val
NM_000545.8:c.1472C>T MANE Select	NP_000536.6:p.Ala491Val
NM_001306179.2:c.1472C>T	NP_001293108.2:p.Ala491Val