Canonical Allele Identifier: CA222937258

Gene: BEST1

Linked Data

• dbSNP Id: rs141943573
• gnomAD v4: 11-61957527-AGCTGGGGTGGGAAGG-A
• MyVariant Identifiers: chr11:g.61725000_61725014del (hg19) ; chr11:g.61957528_61957542del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61957531_61957545del , CM000673.2:g.61957531_61957545del	GRCh38
NC_000011.9:g.61725003_61725017del , CM000673.1:g.61725003_61725017del	GRCh37
NC_000011.8:g.61481579_61481593del	NCBI36
NG_009033.1:g.12648_12662del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.714+67_714+81del MANE Select	ENSP00000367282.4:n.714+67_714+81del
ENST00000378043.8:c.714+67_714+81del	ENSP00000367282.4:n.714+67_714+81del
ENST00000449131.6:c.534+67_534+81del	ENSP00000399709.2:n.534+67_534+81del
ENST00000524877.5:n.1146+67_1146+81del
ENST00000524926.5:c.714+67_714+81del	ENSP00000432681.1:n.714+67_714+81del
ENST00000526988.1:c.396+67_396+81del	ENSP00000433195.1:n.396+67_396+81del
ENST00000529265.5:n.637+67_637+81del
ENST00000534553.5:c.163+1580_163+1594del	ENSP00000431189.1:n.163+1580_163+1594del
NM_001139443.1:c.534+67_534+81del	NP_001132915.1:n.534+67_534+81del
NM_001300786.1:c.534+67_534+81del	NP_001287715.1:n.534+67_534+81del
NM_001300787.1:c.534+67_534+81del	NP_001287716.1:n.534+67_534+81del
NM_004183.3:c.714+67_714+81del	NP_004174.1:n.714+67_714+81del
XM_005274210.2:c.714+67_714+81del	XP_005274267.1:n.714+67_714+81del
XM_005274215.2:c.396+67_396+81del	XP_005274272.1:n.396+67_396+81del
XM_005274216.2:c.534+67_534+81del	XP_005274273.1:n.534+67_534+81del
XM_005274218.3:c.396+67_396+81del	XP_005274275.1:n.396+67_396+81del
XM_005274219.2:c.714+67_714+81del	XP_005274276.1:n.714+67_714+81del
XM_005274221.2:c.714+67_714+81del	XP_005274278.1:n.714+67_714+81del
XM_011545229.1:c.714+67_714+81del	XP_011543531.1:n.714+67_714+81del
XM_011545230.1:c.621+67_621+81del	XP_011543532.1:n.621+67_621+81del
XM_011545231.1:c.396+67_396+81del	XP_011543533.1:n.396+67_396+81del
XM_011545232.1:c.714+67_714+81del	XP_011543534.1:n.714+67_714+81del
NM_001363591.1:c.396+67_396+81del	NP_001350520.1:n.396+67_396+81del
NM_001363592.1:c.714+67_714+81del	NP_001350521.1:n.714+67_714+81del
NM_001363593.1:c.-462+67_-462+81del	NP_001350522.1:n.-462+67_-462+81del
NR_134580.1:n.1294+67_1294+81del
XM_005274210.4:c.714+67_714+81del	XP_005274267.1:n.714+67_714+81del
XM_005274215.4:c.396+67_396+81del	XP_005274272.1:n.396+67_396+81del
XM_005274216.4:c.534+67_534+81del	XP_005274273.1:n.534+67_534+81del
XM_005274219.4:c.714+67_714+81del	XP_005274276.1:n.714+67_714+81del
XM_005274221.4:c.714+67_714+81del	XP_005274278.1:n.714+67_714+81del
XM_011545229.3:c.714+67_714+81del	XP_011543531.1:n.714+67_714+81del
XM_011545230.3:c.621+67_621+81del	XP_011543532.1:n.621+67_621+81del
XM_017018230.2:c.396+67_396+81del	XP_016873719.1:n.396+67_396+81del
XR_001747952.2:n.1212+67_1212+81del
XR_001747953.2:n.1404+67_1404+81del
XR_001747954.2:n.1404+67_1404+81del
XR_001748245.1:n.1187_1201del
XR_002957249.1:n.506-310_506-296del
NM_004183.4:c.714+67_714+81del MANE Select	NP_004174.1:n.714+67_714+81del
NM_001139443.2:c.534+67_534+81del	NP_001132915.1:n.534+67_534+81del
NM_001300786.2:c.534+67_534+81del	NP_001287715.1:n.534+67_534+81del
NM_001300787.2:c.534+67_534+81del	NP_001287716.1:n.534+67_534+81del
NM_001363591.2:c.396+67_396+81del	NP_001350520.1:n.396+67_396+81del
NM_001363593.2:c.-462+67_-462+81del	NP_001350522.1:n.-462+67_-462+81del
NR_134580.2:n.827+67_827+81del