Canonical Allele Identifier: CA380846288

Gene: BEST1 FTH1

Linked Data

• COSMIC: COSM1355299 ; COSM1355300
• MyVariant Identifiers: chr11:g.61727461C>A (hg19) ; chr11:g.61959989C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959989C>A , CM000673.2:g.61959989C>A	GRCh38
NC_000011.9:g.61727461C>A , CM000673.1:g.61727461C>A	GRCh37
NC_000011.8:g.61484037C>A	NCBI36
NG_009033.1:g.15106C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.1046C>A (BEST1) MANE Select	ENSP00000367282.4:p.Ala349Asp
ENST00000378043.8:c.1046C>A (BEST1)	ENSP00000367282.4:p.Ala349Asp
ENST00000449131.6:c.866C>A (BEST1)	ENSP00000399709.2:p.Ala289Asp
ENST00000524877.5:n.2677C>A (BEST1)
ENST00000524926.5:c.1249C>A (BEST1)	ENSP00000432681.1:p.Leu417Met
ENST00000526988.1:c.931C>A (BEST1)	ENSP00000433195.1:p.Leu311Met
ENST00000529191.5:c.115-62G>T (FTH1)	ENSP00000431659.1:n.115-62G>T
ENST00000529631.5:c.115-85G>T (FTH1)	ENSP00000431575.1:n.115-85G>T
ENST00000530019.5:c.262-85G>T (FTH1)	ENSP00000433470.1:n.262-85G>T
ENST00000534553.5:c.164-2266C>A (BEST1)	ENSP00000431189.1:n.164-2266C>A
NM_001139443.1:c.866C>A (BEST1)	NP_001132915.1:p.Ala289Asp
NM_001300786.1:c.785C>A (BEST1)	NP_001287715.1:p.Ala262Asp
NM_001300787.1:c.866C>A (BEST1)	NP_001287716.1:p.Ala289Asp
NM_004183.3:c.1046C>A (BEST1)	NP_004174.1:p.Ala349Asp
XM_005274210.2:c.1046C>A (BEST1)	XP_005274267.1:p.Ala349Asp
XM_005274215.2:c.728C>A (BEST1)	XP_005274272.1:p.Ala243Asp
XM_005274216.2:c.1069C>A (BEST1)	XP_005274273.1:p.Leu357Met
XM_005274218.3:c.931C>A (BEST1)	XP_005274275.1:p.Leu311Met
XM_005274219.2:c.867+1691C>A (BEST1)	XP_005274276.1:n.867+1691C>A
XM_005274221.2:c.715-2266C>A (BEST1)	XP_005274278.1:n.715-2266C>A
XM_011545229.1:c.1046C>A (BEST1)	XP_011543531.1:p.Ala349Asp
XM_011545230.1:c.953C>A (BEST1)	XP_011543532.1:p.Ala318Asp
XM_011545231.1:c.728C>A (BEST1)	XP_011543533.1:p.Ala243Asp
XM_011545232.1:c.1249C>A (BEST1)	XP_011543534.1:p.Leu417Met
XM_011545233.1:c.203C>A (BEST1)	XP_011543535.1:p.Ala68Asp
NM_001363591.1:c.728C>A (BEST1)	NP_001350520.1:p.Ala243Asp
NM_001363592.1:c.1249C>A (BEST1)	NP_001350521.1:p.Leu417Met
NM_001363593.1:c.74C>A (BEST1)	NP_001350522.1:p.Ala25Asp
NR_134580.1:n.1829C>A (BEST1)
XM_005274210.4:c.1046C>A (BEST1)	XP_005274267.1:p.Ala349Asp
XM_005274215.4:c.728C>A (BEST1)	XP_005274272.1:p.Ala243Asp
XM_005274216.4:c.1069C>A (BEST1)	XP_005274273.1:p.Leu357Met
XM_005274219.4:c.867+1691C>A (BEST1)	XP_005274276.1:n.867+1691C>A
XM_005274221.4:c.715-2266C>A (BEST1)	XP_005274278.1:n.715-2266C>A
XM_011545229.3:c.1046C>A (BEST1)	XP_011543531.1:p.Ala349Asp
XM_011545230.3:c.953C>A (BEST1)	XP_011543532.1:p.Ala318Asp
XM_011545233.3:c.203C>A (BEST1)	XP_011543535.1:p.Ala68Asp
XM_017018230.2:c.931C>A (BEST1)	XP_016873719.1:p.Leu311Met
XR_001747952.2:n.1747C>A (BEST1)
XR_001747953.2:n.1557+1691C>A (BEST1)
XR_001747954.2:n.1405-2266C>A (BEST1)
NM_004183.4:c.1046C>A (BEST1) MANE Select	NP_004174.1:p.Ala349Asp
NM_001139443.2:c.866C>A (BEST1)	NP_001132915.1:p.Ala289Asp
NM_001300786.2:c.785C>A (BEST1)	NP_001287715.1:p.Ala262Asp
NM_001300787.2:c.866C>A (BEST1)	NP_001287716.1:p.Ala289Asp
NM_001363591.2:c.728C>A (BEST1)	NP_001350520.1:p.Ala243Asp
NM_001363593.2:c.74C>A (BEST1)	NP_001350522.1:p.Ala25Asp
NR_134580.2:n.1362C>A (BEST1)