Canonical Allele Identifier: CA380846312

Gene: BEST1 FTH1

Linked Data

• MyVariant Identifiers: chr11:g.61727469G>T (hg19) ; chr11:g.61959997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959997G>T , CM000673.2:g.61959997G>T	GRCh38
NC_000011.9:g.61727469G>T , CM000673.1:g.61727469G>T	GRCh37
NC_000011.8:g.61484045G>T	NCBI36
NG_009033.1:g.15114G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.1054G>T (BEST1) MANE Select	ENSP00000367282.4:p.Ala352Ser
ENST00000378043.8:c.1054G>T (BEST1)	ENSP00000367282.4:p.Ala352Ser
ENST00000449131.6:c.874G>T (BEST1)	ENSP00000399709.2:p.Ala292Ser
ENST00000524877.5:n.2685G>T (BEST1)
ENST00000524926.5:c.1257G>T (BEST1)	ENSP00000432681.1:p.Pro419=
ENST00000526988.1:c.939G>T (BEST1)	ENSP00000433195.1:p.Pro313=
ENST00000529191.5:c.115-70C>A (FTH1)	ENSP00000431659.1:n.115-70C>A
ENST00000529631.5:c.115-93C>A (FTH1)	ENSP00000431575.1:n.115-93C>A
ENST00000530019.5:c.262-93C>A (FTH1)	ENSP00000433470.1:n.262-93C>A
ENST00000534553.5:c.164-2258G>T (BEST1)	ENSP00000431189.1:n.164-2258G>T
NM_001139443.1:c.874G>T (BEST1)	NP_001132915.1:p.Ala292Ser
NM_001300786.1:c.793G>T (BEST1)	NP_001287715.1:p.Ala265Ser
NM_001300787.1:c.874G>T (BEST1)	NP_001287716.1:p.Ala292Ser
NM_004183.3:c.1054G>T (BEST1)	NP_004174.1:p.Ala352Ser
XM_005274210.2:c.1054G>T (BEST1)	XP_005274267.1:p.Ala352Ser
XM_005274215.2:c.736G>T (BEST1)	XP_005274272.1:p.Ala246Ser
XM_005274216.2:c.1077G>T (BEST1)	XP_005274273.1:p.Pro359=
XM_005274218.3:c.939G>T (BEST1)	XP_005274275.1:p.Pro313=
XM_005274219.2:c.867+1699G>T (BEST1)	XP_005274276.1:n.867+1699G>T
XM_005274221.2:c.715-2258G>T (BEST1)	XP_005274278.1:n.715-2258G>T
XM_011545229.1:c.1054G>T (BEST1)	XP_011543531.1:p.Ala352Ser
XM_011545230.1:c.961G>T (BEST1)	XP_011543532.1:p.Ala321Ser
XM_011545231.1:c.736G>T (BEST1)	XP_011543533.1:p.Ala246Ser
XM_011545232.1:c.1257G>T (BEST1)	XP_011543534.1:p.Pro419=
XM_011545233.1:c.211G>T (BEST1)	XP_011543535.1:p.Ala71Ser
NM_001363591.1:c.736G>T (BEST1)	NP_001350520.1:p.Ala246Ser
NM_001363592.1:c.1257G>T (BEST1)	NP_001350521.1:p.Pro419=
NM_001363593.1:c.82G>T (BEST1)	NP_001350522.1:p.Ala28Ser
NR_134580.1:n.1837G>T (BEST1)
XM_005274210.4:c.1054G>T (BEST1)	XP_005274267.1:p.Ala352Ser
XM_005274215.4:c.736G>T (BEST1)	XP_005274272.1:p.Ala246Ser
XM_005274216.4:c.1077G>T (BEST1)	XP_005274273.1:p.Pro359=
XM_005274219.4:c.867+1699G>T (BEST1)	XP_005274276.1:n.867+1699G>T
XM_005274221.4:c.715-2258G>T (BEST1)	XP_005274278.1:n.715-2258G>T
XM_011545229.3:c.1054G>T (BEST1)	XP_011543531.1:p.Ala352Ser
XM_011545230.3:c.961G>T (BEST1)	XP_011543532.1:p.Ala321Ser
XM_011545233.3:c.211G>T (BEST1)	XP_011543535.1:p.Ala71Ser
XM_017018230.2:c.939G>T (BEST1)	XP_016873719.1:p.Pro313=
XR_001747952.2:n.1755G>T (BEST1)
XR_001747953.2:n.1557+1699G>T (BEST1)
XR_001747954.2:n.1405-2258G>T (BEST1)
NM_004183.4:c.1054G>T (BEST1) MANE Select	NP_004174.1:p.Ala352Ser
NM_001139443.2:c.874G>T (BEST1)	NP_001132915.1:p.Ala292Ser
NM_001300786.2:c.793G>T (BEST1)	NP_001287715.1:p.Ala265Ser
NM_001300787.2:c.874G>T (BEST1)	NP_001287716.1:p.Ala292Ser
NM_001363591.2:c.736G>T (BEST1)	NP_001350520.1:p.Ala246Ser
NM_001363593.2:c.82G>T (BEST1)	NP_001350522.1:p.Ala28Ser
NR_134580.2:n.1370G>T (BEST1)