Canonical Allele Identifier: CA2613931222

Gene: FTH1 BEST1

Linked Data

• gnomAD v4: 11-61964535-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964535G>T , CM000673.2:g.61964535G>T	GRCh38
NC_000011.9:g.61732007G>T , CM000673.1:g.61732007G>T	GRCh37
NC_000011.8:g.61488583G>T	NCBI36
NG_008346.1:g.8126C>A
NG_009033.1:g.19652G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*192C>A (FTH1) MANE Select	ENSP00000273550.7:n.*192C>A
ENST00000273550.11:c.*192C>A (FTH1)	ENSP00000273550.7:n.*192C>A
ENST00000449131.6:c.*1386G>T (BEST1)	ENSP00000399709.2:n.*1386G>T
ENST00000529191.5:c.114+2777C>A (FTH1)	ENSP00000431659.1:n.114+2777C>A
ENST00000529631.5:c.114+2777C>A (FTH1)	ENSP00000431575.1:n.114+2777C>A
ENST00000530019.5:c.261+834C>A (FTH1)	ENSP00000433470.1:n.261+834C>A
NM_002032.2:c.*192C>A (FTH1)	NP_002023.2:n.*192C>A
NM_002032.3:c.*192C>A (FTH1) MANE Select	NP_002023.2:n.*192C>A
NM_001139443.2:c.*1386G>T (BEST1)	NP_001132915.1:n.*1386G>T
NM_001363591.2:c.*1386G>T (BEST1)	NP_001350520.1:n.*1386G>T
NM_001363593.2:c.*1386G>T (BEST1)	NP_001350522.1:n.*1386G>T