Canonical Allele Identifier: CA474958816

Gene: FTH1 BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61732462G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964990G>T , CM000673.2:g.61964990G>T	GRCh38
NC_000011.9:g.61732462G>T , CM000673.1:g.61732462G>T	GRCh37
NC_000011.8:g.61489038G>T	NCBI36
NG_008346.1:g.7671C>A
NG_009033.1:g.20107G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000620041.5:c.384C>A (FTH1)	ENSP00000484477.1:p.Pro128=
ENST00000273550.12:c.384C>A (FTH1) MANE Select	ENSP00000273550.7:p.Pro128=
ENST00000273550.11:c.384C>A (FTH1)	ENSP00000273550.7:p.Pro128=
ENST00000449131.6:c.*1841G>T (BEST1)	ENSP00000399709.2:n.*1841G>T
ENST00000526640.5:c.294C>A (FTH1)	ENSP00000433321.1:p.Pro98=
ENST00000529191.5:c.114+2322C>A (FTH1)	ENSP00000431659.1:n.114+2322C>A
ENST00000529548.1:c.174C>A (FTH1)	ENSP00000436947.1:p.Pro58=
ENST00000529631.5:c.114+2322C>A (FTH1)	ENSP00000431575.1:n.114+2322C>A
ENST00000530019.5:c.261+379C>A (FTH1)	ENSP00000433470.1:n.261+379C>A
ENST00000532601.1:c.174C>A (FTH1)	ENSP00000435111.1:p.Pro58=
ENST00000532829.5:c.*89C>A (FTH1)	ENSP00000432223.1:n.*89C>A
ENST00000533138.1:n.828C>A (FTH1)
ENST00000534180.1:c.*293C>A (FTH1)	ENSP00000434403.1:n.*293C>A
ENST00000534719.1:n.545C>A (FTH1)
ENST00000620041.4:c.384C>A (FTH1)	ENSP00000484477.1:p.Pro128=
NM_002032.2:c.384C>A (FTH1)	NP_002023.2:p.Pro128=
NM_002032.3:c.384C>A (FTH1) MANE Select	NP_002023.2:p.Pro128=
NM_001139443.2:c.*1841G>T (BEST1)	NP_001132915.1:n.*1841G>T
NM_001363591.2:c.*1841G>T (BEST1)	NP_001350520.1:n.*1841G>T
NM_001363593.2:c.*1841G>T (BEST1)	NP_001350522.1:n.*1841G>T