Canonical Allele Identifier: CA380853897

Gene: FTH1 BEST1

Linked Data

• dbSNP Id: rs1942404420
• gnomAD v4: 11-61964802-C-T
• MyVariant Identifiers: chr11:g.61732274C>T (hg19) ; chr11:g.61964802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964802C>T , CM000673.2:g.61964802C>T	GRCh38
NC_000011.9:g.61732274C>T , CM000673.1:g.61732274C>T	GRCh37
NC_000011.8:g.61488850C>T	NCBI36
NG_008346.1:g.7859G>A
NG_009033.1:g.19919C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620041.5:c.477G>A (FTH1)	ENSP00000484477.1:p.Met159Ile
ENST00000273550.12:c.477G>A (FTH1) MANE Select	ENSP00000273550.7:p.Met159Ile
ENST00000273550.11:c.477G>A (FTH1)	ENSP00000273550.7:p.Met159Ile
ENST00000449131.6:c.*1653C>T (BEST1)	ENSP00000399709.2:n.*1653C>T
ENST00000526640.5:c.387G>A (FTH1)	ENSP00000433321.1:p.Met129Ile
ENST00000529191.5:c.114+2510G>A (FTH1)	ENSP00000431659.1:n.114+2510G>A
ENST00000529631.5:c.114+2510G>A (FTH1)	ENSP00000431575.1:n.114+2510G>A
ENST00000530019.5:c.261+567G>A (FTH1)	ENSP00000433470.1:n.261+567G>A
ENST00000532601.1:c.267G>A (FTH1)	ENSP00000435111.1:p.Met89Ile
ENST00000532829.5:c.*182G>A (FTH1)	ENSP00000432223.1:n.*182G>A
ENST00000534180.1:c.*386G>A (FTH1)	ENSP00000434403.1:n.*386G>A
ENST00000534719.1:n.733G>A (FTH1)
ENST00000620041.4:c.477G>A (FTH1)	ENSP00000484477.1:p.Met159Ile
NM_002032.2:c.477G>A (FTH1)	NP_002023.2:p.Met159Ile
NM_002032.3:c.477G>A (FTH1) MANE Select	NP_002023.2:p.Met159Ile
NM_001139443.2:c.*1653C>T (BEST1)	NP_001132915.1:n.*1653C>T
NM_001363591.2:c.*1653C>T (BEST1)	NP_001350520.1:n.*1653C>T
NM_001363593.2:c.*1653C>T (BEST1)	NP_001350522.1:n.*1653C>T