Canonical Allele Identifier: CA386968033

Gene: HNF1A

Linked Data

• MyVariant Identifiers: chr12:g.121434112T>G (hg19) ; chr12:g.120996309T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996309T>G , CM000674.2:g.120996309T>G	GRCh38
NC_000012.11:g.121434112T>G , CM000674.1:g.121434112T>G	GRCh37
NC_000012.10:g.119918495T>G	NCBI36
NG_011731.2:g.22564T>G , LRG_522:g.22564T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.751-74T>G	ENSP00000453965.2:n.751-74T>G
ENST00000257555.11:c.1003T>G MANE Select	ENSP00000257555.5:p.Ser335Ala
ENST00000257555.10:c.1003T>G	ENSP00000257555.4:p.Ser335Ala
ENST00000400024.6:c.1003T>G	ENSP00000476181.1:p.Ser335Ala
ENST00000402929.5:n.1138T>G
ENST00000535955.5:n.43-1182T>G
ENST00000538626.2:n.191-1182T>G
ENST00000538646.5:c.816T>G	ENSP00000443964.1:p.Pro272=
ENST00000540108.1:c.*443T>G	ENSP00000445445.1:n.*443T>G
ENST00000541395.5:c.1003T>G	ENSP00000443112.1:p.Ser335Ala
ENST00000541924.5:c.*17T>G	ENSP00000440361.1:n.*17T>G
ENST00000543427.5:c.634-295T>G	ENSP00000439721.2:n.634-295T>G
ENST00000544413.2:c.1003T>G	ENSP00000438804.1:p.Ser335Ala
ENST00000544574.5:c.73-308T>G	ENSP00000438565.1:n.73-308T>G
ENST00000560968.5:c.894-74T>G
ENST00000615446.4:c.-210T>G	ENSP00000483994.1:n.-210T>G
ENST00000617366.4:c.587-1325T>G	ENSP00000481967.1:n.587-1325T>G
NM_000545.5:c.1003T>G , LRG_522t1:c.1003T>G	NP_000536.5:p.Ser335Ala
NM_000545.6:c.1003T>G	NP_000536.5:p.Ser335Ala
NM_001306179.1:c.1003T>G	NP_001293108.1:p.Ser335Ala
XM_005253931.2:c.1003T>G	XP_005253988.1:p.Ser335Ala
XM_024449168.1:c.1003T>G	XP_024304936.1:p.Ser335Ala
NM_000545.8:c.1003T>G MANE Select	NP_000536.6:p.Ser335Ala
NM_001306179.2:c.1003T>G	NP_001293108.2:p.Ser335Ala