Canonical Allele Identifier: CA222946015

Gene: FTH1 BEST1

Linked Data

• dbSNP Id: rs1038190831
• MyVariant Identifiers: chr11:g.61732010T>G (hg19) ; chr11:g.61964538T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964538T>G , CM000673.2:g.61964538T>G	GRCh38
NC_000011.9:g.61732010T>G , CM000673.1:g.61732010T>G	GRCh37
NC_000011.8:g.61488586T>G	NCBI36
NG_008346.1:g.8123A>C
NG_009033.1:g.19655T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*189A>C (FTH1) MANE Select	ENSP00000273550.7:n.*189A>C
ENST00000273550.11:c.*189A>C (FTH1)	ENSP00000273550.7:n.*189A>C
ENST00000449131.6:c.*1389T>G (BEST1)	ENSP00000399709.2:n.*1389T>G
ENST00000529191.5:c.114+2774A>C (FTH1)	ENSP00000431659.1:n.114+2774A>C
ENST00000529631.5:c.114+2774A>C (FTH1)	ENSP00000431575.1:n.114+2774A>C
ENST00000530019.5:c.261+831A>C (FTH1)	ENSP00000433470.1:n.261+831A>C
NM_002032.2:c.*189A>C (FTH1)	NP_002023.2:n.*189A>C
NM_002032.3:c.*189A>C (FTH1) MANE Select	NP_002023.2:n.*189A>C
NM_001139443.2:c.*1389T>G (BEST1)	NP_001132915.1:n.*1389T>G
NM_001363591.2:c.*1389T>G (BEST1)	NP_001350520.1:n.*1389T>G
NM_001363593.2:c.*1389T>G (BEST1)	NP_001350522.1:n.*1389T>G