Canonical Allele Identifier: CA380846384

Gene: BEST1 FTH1

Linked Data

• MyVariant Identifiers: chr11:g.61727495G>C (hg19) ; chr11:g.61960023G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61960023G>C , CM000673.2:g.61960023G>C	GRCh38
NC_000011.9:g.61727495G>C , CM000673.1:g.61727495G>C	GRCh37
NC_000011.8:g.61484071G>C	NCBI36
NG_009033.1:g.15140G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.1080G>C (BEST1) MANE Select	ENSP00000367282.4:p.Met360Ile
ENST00000378043.8:c.1080G>C (BEST1)	ENSP00000367282.4:p.Met360Ile
ENST00000449131.6:c.900G>C (BEST1)	ENSP00000399709.2:p.Met300Ile
ENST00000524877.5:n.2711G>C (BEST1)
ENST00000524926.5:c.1283G>C (BEST1)	ENSP00000432681.1:p.Trp428Ser
ENST00000526988.1:c.965G>C (BEST1)	ENSP00000433195.1:p.Trp322Ser
ENST00000529191.5:c.115-96C>G (FTH1)	ENSP00000431659.1:n.115-96C>G
ENST00000529631.5:c.115-119C>G (FTH1)	ENSP00000431575.1:n.115-119C>G
ENST00000530019.5:c.262-119C>G (FTH1)	ENSP00000433470.1:n.262-119C>G
ENST00000534553.5:c.164-2232G>C (BEST1)	ENSP00000431189.1:n.164-2232G>C
NM_001139443.1:c.900G>C (BEST1)	NP_001132915.1:p.Met300Ile
NM_001300786.1:c.819G>C (BEST1)	NP_001287715.1:p.Met273Ile
NM_001300787.1:c.900G>C (BEST1)	NP_001287716.1:p.Met300Ile
NM_004183.3:c.1080G>C (BEST1)	NP_004174.1:p.Met360Ile
XM_005274210.2:c.1080G>C (BEST1)	XP_005274267.1:p.Met360Ile
XM_005274215.2:c.762G>C (BEST1)	XP_005274272.1:p.Met254Ile
XM_005274216.2:c.1103G>C (BEST1)	XP_005274273.1:p.Trp368Ser
XM_005274218.3:c.965G>C (BEST1)	XP_005274275.1:p.Trp322Ser
XM_005274219.2:c.867+1725G>C (BEST1)	XP_005274276.1:n.867+1725G>C
XM_005274221.2:c.715-2232G>C (BEST1)	XP_005274278.1:n.715-2232G>C
XM_011545229.1:c.1080G>C (BEST1)	XP_011543531.1:p.Met360Ile
XM_011545230.1:c.987G>C (BEST1)	XP_011543532.1:p.Met329Ile
XM_011545231.1:c.762G>C (BEST1)	XP_011543533.1:p.Met254Ile
XM_011545232.1:c.1283G>C (BEST1)	XP_011543534.1:p.Trp428Ser
XM_011545233.1:c.237G>C (BEST1)	XP_011543535.1:p.Met79Ile
NM_001363591.1:c.762G>C (BEST1)	NP_001350520.1:p.Met254Ile
NM_001363592.1:c.1283G>C (BEST1)	NP_001350521.1:p.Trp428Ser
NM_001363593.1:c.108G>C (BEST1)	NP_001350522.1:p.Met36Ile
NR_134580.1:n.1863G>C (BEST1)
XM_005274210.4:c.1080G>C (BEST1)	XP_005274267.1:p.Met360Ile
XM_005274215.4:c.762G>C (BEST1)	XP_005274272.1:p.Met254Ile
XM_005274216.4:c.1103G>C (BEST1)	XP_005274273.1:p.Trp368Ser
XM_005274219.4:c.867+1725G>C (BEST1)	XP_005274276.1:n.867+1725G>C
XM_005274221.4:c.715-2232G>C (BEST1)	XP_005274278.1:n.715-2232G>C
XM_011545229.3:c.1080G>C (BEST1)	XP_011543531.1:p.Met360Ile
XM_011545230.3:c.987G>C (BEST1)	XP_011543532.1:p.Met329Ile
XM_011545233.3:c.237G>C (BEST1)	XP_011543535.1:p.Met79Ile
XM_017018230.2:c.965G>C (BEST1)	XP_016873719.1:p.Trp322Ser
XR_001747952.2:n.1781G>C (BEST1)
XR_001747953.2:n.1557+1725G>C (BEST1)
XR_001747954.2:n.1405-2232G>C (BEST1)
NM_004183.4:c.1080G>C (BEST1) MANE Select	NP_004174.1:p.Met360Ile
NM_001139443.2:c.900G>C (BEST1)	NP_001132915.1:p.Met300Ile
NM_001300786.2:c.819G>C (BEST1)	NP_001287715.1:p.Met273Ile
NM_001300787.2:c.900G>C (BEST1)	NP_001287716.1:p.Met300Ile
NM_001363591.2:c.762G>C (BEST1)	NP_001350520.1:p.Met254Ile
NM_001363593.2:c.108G>C (BEST1)	NP_001350522.1:p.Met36Ile
NR_134580.2:n.1396G>C (BEST1)