Canonical Allele Identifier: CA380840586

Gene: BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61725790T>A (hg19) ; chr11:g.61958318T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61958318T>A , CM000673.2:g.61958318T>A	GRCh38
NC_000011.9:g.61725790T>A , CM000673.1:g.61725790T>A	GRCh37
NC_000011.8:g.61482366T>A	NCBI36
NG_009033.1:g.13435T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.867+20T>A MANE Select	ENSP00000367282.4:n.867+20T>A
ENST00000378043.8:c.867+20T>A	ENSP00000367282.4:n.867+20T>A
ENST00000449131.6:c.687+20T>A	ENSP00000399709.2:n.687+20T>A
ENST00000524877.5:n.1319T>A
ENST00000524926.5:c.887T>A	ENSP00000432681.1:p.Leu296Gln
ENST00000526988.1:c.569T>A	ENSP00000433195.1:p.Leu190Gln
ENST00000529265.5:n.810T>A
ENST00000534553.5:c.163+2367T>A	ENSP00000431189.1:n.163+2367T>A
NM_001139443.1:c.687+20T>A	NP_001132915.1:n.687+20T>A
NM_001300786.1:c.687+20T>A	NP_001287715.1:n.687+20T>A
NM_001300787.1:c.687+20T>A	NP_001287716.1:n.687+20T>A
NM_004183.3:c.867+20T>A	NP_004174.1:n.867+20T>A
XM_005274210.2:c.867+20T>A	XP_005274267.1:n.867+20T>A
XM_005274215.2:c.549+20T>A	XP_005274272.1:n.549+20T>A
XM_005274216.2:c.707T>A	XP_005274273.1:p.Leu236Gln
XM_005274218.3:c.569T>A	XP_005274275.1:p.Leu190Gln
XM_005274219.2:c.867+20T>A	XP_005274276.1:n.867+20T>A
XM_005274221.2:c.714+854T>A	XP_005274278.1:n.714+854T>A
XM_011545229.1:c.867+20T>A	XP_011543531.1:n.867+20T>A
XM_011545230.1:c.774+20T>A	XP_011543532.1:n.774+20T>A
XM_011545231.1:c.549+20T>A	XP_011543533.1:n.549+20T>A
XM_011545232.1:c.887T>A	XP_011543534.1:p.Leu296Gln
NM_001363591.1:c.549+20T>A	NP_001350520.1:n.549+20T>A
NM_001363592.1:c.887T>A	NP_001350521.1:p.Leu296Gln
NM_001363593.1:c.-289T>A	NP_001350522.1:n.-289T>A
NR_134580.1:n.1467T>A
XM_005274210.4:c.867+20T>A	XP_005274267.1:n.867+20T>A
XM_005274215.4:c.549+20T>A	XP_005274272.1:n.549+20T>A
XM_005274216.4:c.707T>A	XP_005274273.1:p.Leu236Gln
XM_005274219.4:c.867+20T>A	XP_005274276.1:n.867+20T>A
XM_005274221.4:c.714+854T>A	XP_005274278.1:n.714+854T>A
XM_011545229.3:c.867+20T>A	XP_011543531.1:n.867+20T>A
XM_011545230.3:c.774+20T>A	XP_011543532.1:n.774+20T>A
XM_017018230.2:c.569T>A	XP_016873719.1:p.Leu190Gln
XR_001747952.2:n.1385T>A
XR_001747953.2:n.1557+20T>A
XR_001747954.2:n.1404+854T>A
XR_001748245.1:n.411A>T
XR_002957249.1:n.411A>T
NM_004183.4:c.867+20T>A MANE Select	NP_004174.1:n.867+20T>A
NM_001139443.2:c.687+20T>A	NP_001132915.1:n.687+20T>A
NM_001300786.2:c.687+20T>A	NP_001287715.1:n.687+20T>A
NM_001300787.2:c.687+20T>A	NP_001287716.1:n.687+20T>A
NM_001363591.2:c.549+20T>A	NP_001350520.1:n.549+20T>A
NM_001363593.2:c.-289T>A	NP_001350522.1:n.-289T>A
NR_134580.2:n.1000T>A