Canonical Allele Identifier: CA474557062

Gene: BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61722645C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61955173C>T , CM000673.2:g.61955173C>T	GRCh38
NC_000011.9:g.61722645C>T , CM000673.1:g.61722645C>T	GRCh37
NC_000011.8:g.61479221C>T	NCBI36
NG_009033.1:g.10290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.219C>T MANE Select	ENSP00000367282.4:p.Ile73=
ENST00000378043.8:c.219C>T	ENSP00000367282.4:p.Ile73=
ENST00000449131.6:c.39C>T	ENSP00000399709.2:p.Ile13=
ENST00000524877.5:n.135C>T
ENST00000524926.5:c.219C>T	ENSP00000432681.1:p.Ile73=
ENST00000526988.1:c.-145C>T	ENSP00000433195.1:n.-145C>T
ENST00000529265.5:n.142C>T
ENST00000533521.5:n.327C>T
ENST00000534553.5:c.-145C>T	ENSP00000431189.1:n.-145C>T
NM_001139443.1:c.39C>T	NP_001132915.1:p.Ile13=
NM_001300786.1:c.39C>T	NP_001287715.1:p.Ile13=
NM_001300787.1:c.39C>T	NP_001287716.1:p.Ile13=
NM_004183.3:c.219C>T	NP_004174.1:p.Ile73=
XM_005274210.2:c.219C>T	XP_005274267.1:p.Ile73=
XM_005274216.2:c.39C>T	XP_005274273.1:p.Ile13=
XM_005274218.3:c.-145C>T	XP_005274275.1:n.-145C>T
XM_005274219.2:c.219C>T	XP_005274276.1:p.Ile73=
XM_005274221.2:c.219C>T	XP_005274278.1:p.Ile73=
XM_011545229.1:c.219C>T	XP_011543531.1:p.Ile73=
XM_011545230.1:c.126C>T	XP_011543532.1:p.Ile42=
XM_011545231.1:c.-145C>T	XP_011543533.1:n.-145C>T
XM_011545232.1:c.219C>T	XP_011543534.1:p.Ile73=
NM_001363591.1:c.-286C>T	NP_001350520.1:n.-286C>T
NM_001363592.1:c.219C>T	NP_001350521.1:p.Ile73=
NM_001363593.1:c.-1143C>T	NP_001350522.1:n.-1143C>T
NR_134580.1:n.799C>T
XM_005274210.4:c.219C>T	XP_005274267.1:p.Ile73=
XM_005274215.4:c.-286C>T	XP_005274272.1:n.-286C>T
XM_005274216.4:c.39C>T	XP_005274273.1:p.Ile13=
XM_005274219.4:c.219C>T	XP_005274276.1:p.Ile73=
XM_005274221.4:c.219C>T	XP_005274278.1:p.Ile73=
XM_011545229.3:c.219C>T	XP_011543531.1:p.Ile73=
XM_011545230.3:c.126C>T	XP_011543532.1:p.Ile42=
XM_017018230.2:c.-286C>T	XP_016873719.1:n.-286C>T
XR_001747952.2:n.717C>T
XR_001747953.2:n.909C>T
XR_001747954.2:n.909C>T
XR_002957249.1:n.2565G>A
NM_004183.4:c.219C>T MANE Select	NP_004174.1:p.Ile73=
NM_001139443.2:c.39C>T	NP_001132915.1:p.Ile13=
NM_001300786.2:c.39C>T	NP_001287715.1:p.Ile13=
NM_001300787.2:c.39C>T	NP_001287716.1:p.Ile13=
NR_134580.2:n.332C>T