Canonical Allele Identifier: CA380846183

Gene: BEST1 FTH1

Linked Data

• ClinVar Variation Id: 3133723
• ClinVar RCV Id: RCV004429009
• gnomAD v4: 11-61959949-A-G
• MyVariant Identifiers: chr11:g.61727421A>G (hg19) ; chr11:g.61959949A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959949A>G , CM000673.2:g.61959949A>G	GRCh38
NC_000011.9:g.61727421A>G , CM000673.1:g.61727421A>G	GRCh37
NC_000011.8:g.61483997A>G	NCBI36
NG_009033.1:g.15066A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.1006A>G (BEST1) MANE Select	ENSP00000367282.4:p.Met336Val
ENST00000378043.8:c.1006A>G (BEST1)	ENSP00000367282.4:p.Met336Val
ENST00000449131.6:c.826A>G (BEST1)	ENSP00000399709.2:p.Met276Val
ENST00000524877.5:n.2637A>G (BEST1)
ENST00000524926.5:c.1209A>G (BEST1)	ENSP00000432681.1:p.Thr403=
ENST00000526988.1:c.891A>G (BEST1)	ENSP00000433195.1:p.Thr297=
ENST00000529191.5:c.115-22T>C (FTH1)	ENSP00000431659.1:n.115-22T>C
ENST00000529631.5:c.115-45T>C (FTH1)	ENSP00000431575.1:n.115-45T>C
ENST00000530019.5:c.262-45T>C (FTH1)	ENSP00000433470.1:n.262-45T>C
ENST00000534553.5:c.164-2306A>G (BEST1)	ENSP00000431189.1:n.164-2306A>G
NM_001139443.1:c.826A>G (BEST1)	NP_001132915.1:p.Met276Val
NM_001300786.1:c.745A>G (BEST1)	NP_001287715.1:p.Met249Val
NM_001300787.1:c.826A>G (BEST1)	NP_001287716.1:p.Met276Val
NM_004183.3:c.1006A>G (BEST1)	NP_004174.1:p.Met336Val
XM_005274210.2:c.1006A>G (BEST1)	XP_005274267.1:p.Met336Val
XM_005274215.2:c.688A>G (BEST1)	XP_005274272.1:p.Met230Val
XM_005274216.2:c.1029A>G (BEST1)	XP_005274273.1:p.Thr343=
XM_005274218.3:c.891A>G (BEST1)	XP_005274275.1:p.Thr297=
XM_005274219.2:c.867+1651A>G (BEST1)	XP_005274276.1:n.867+1651A>G
XM_005274221.2:c.715-2306A>G (BEST1)	XP_005274278.1:n.715-2306A>G
XM_011545229.1:c.1006A>G (BEST1)	XP_011543531.1:p.Met336Val
XM_011545230.1:c.913A>G (BEST1)	XP_011543532.1:p.Met305Val
XM_011545231.1:c.688A>G (BEST1)	XP_011543533.1:p.Met230Val
XM_011545232.1:c.1209A>G (BEST1)	XP_011543534.1:p.Thr403=
XM_011545233.1:c.163A>G (BEST1)	XP_011543535.1:p.Met55Val
NM_001363591.1:c.688A>G (BEST1)	NP_001350520.1:p.Met230Val
NM_001363592.1:c.1209A>G (BEST1)	NP_001350521.1:p.Thr403=
NM_001363593.1:c.34A>G (BEST1)	NP_001350522.1:p.Met12Val
NR_134580.1:n.1789A>G (BEST1)
XM_005274210.4:c.1006A>G (BEST1)	XP_005274267.1:p.Met336Val
XM_005274215.4:c.688A>G (BEST1)	XP_005274272.1:p.Met230Val
XM_005274216.4:c.1029A>G (BEST1)	XP_005274273.1:p.Thr343=
XM_005274219.4:c.867+1651A>G (BEST1)	XP_005274276.1:n.867+1651A>G
XM_005274221.4:c.715-2306A>G (BEST1)	XP_005274278.1:n.715-2306A>G
XM_011545229.3:c.1006A>G (BEST1)	XP_011543531.1:p.Met336Val
XM_011545230.3:c.913A>G (BEST1)	XP_011543532.1:p.Met305Val
XM_011545233.3:c.163A>G (BEST1)	XP_011543535.1:p.Met55Val
XM_017018230.2:c.891A>G (BEST1)	XP_016873719.1:p.Thr297=
XR_001747952.2:n.1707A>G (BEST1)
XR_001747953.2:n.1557+1651A>G (BEST1)
XR_001747954.2:n.1405-2306A>G (BEST1)
NM_004183.4:c.1006A>G (BEST1) MANE Select	NP_004174.1:p.Met336Val
NM_001139443.2:c.826A>G (BEST1)	NP_001132915.1:p.Met276Val
NM_001300786.2:c.745A>G (BEST1)	NP_001287715.1:p.Met249Val
NM_001300787.2:c.826A>G (BEST1)	NP_001287716.1:p.Met276Val
NM_001363591.2:c.688A>G (BEST1)	NP_001350520.1:p.Met230Val
NM_001363593.2:c.34A>G (BEST1)	NP_001350522.1:p.Met12Val
NR_134580.2:n.1322A>G (BEST1)