Canonical Allele Identifier: CA1977538962

Gene: FTH1 BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964515G= , CM000673.2:g.61964515G=	GRCh38
NC_000011.9:g.61731987G= , CM000673.1:g.61731987G=	GRCh37
NC_000011.8:g.61488563G=	NCBI36
NG_008346.1:g.8146C=
NG_009033.1:g.19632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*212C= (FTH1) MANE Select	ENSP00000273550.7:n.*212C=
ENST00000273550.11:c.*212C= (FTH1)	ENSP00000273550.7:n.*212C=
ENST00000449131.6:c.*1366G= (BEST1)	ENSP00000399709.2:n.*1366G=
ENST00000529191.5:c.114+2797C= (FTH1)	ENSP00000431659.1:n.114+2797C=
ENST00000529631.5:c.114+2797C= (FTH1)	ENSP00000431575.1:n.114+2797C=
ENST00000530019.5:c.261+854C= (FTH1)	ENSP00000433470.1:n.261+854C=
NM_002032.2:c.*212C= (FTH1)	NP_002023.2:n.*212C=
NM_002032.3:c.*212C= (FTH1) MANE Select	NP_002023.2:n.*212C=
NM_001139443.2:c.*1366G= (BEST1)	NP_001132915.1:n.*1366G=
NM_001363591.2:c.*1366G= (BEST1)	NP_001350520.1:n.*1366G=
NM_001363593.2:c.*1366G= (BEST1)	NP_001350522.1:n.*1366G=