Canonical Allele Identifier: CA380840829

Gene: BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61725827G>T (hg19) ; chr11:g.61958355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61958355G>T , CM000673.2:g.61958355G>T	GRCh38
NC_000011.9:g.61725827G>T , CM000673.1:g.61725827G>T	GRCh37
NC_000011.8:g.61482403G>T	NCBI36
NG_009033.1:g.13472G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.867+57G>T MANE Select	ENSP00000367282.4:n.867+57G>T
ENST00000378043.8:c.867+57G>T	ENSP00000367282.4:n.867+57G>T
ENST00000449131.6:c.687+57G>T	ENSP00000399709.2:n.687+57G>T
ENST00000524877.5:n.1356G>T
ENST00000524926.5:c.924G>T	ENSP00000432681.1:p.Gln308His
ENST00000526988.1:c.606G>T	ENSP00000433195.1:p.Gln202His
ENST00000529265.5:n.847G>T
ENST00000534553.5:c.163+2404G>T	ENSP00000431189.1:n.163+2404G>T
NM_001139443.1:c.687+57G>T	NP_001132915.1:n.687+57G>T
NM_001300786.1:c.687+57G>T	NP_001287715.1:n.687+57G>T
NM_001300787.1:c.687+57G>T	NP_001287716.1:n.687+57G>T
NM_004183.3:c.867+57G>T	NP_004174.1:n.867+57G>T
XM_005274210.2:c.867+57G>T	XP_005274267.1:n.867+57G>T
XM_005274215.2:c.549+57G>T	XP_005274272.1:n.549+57G>T
XM_005274216.2:c.744G>T	XP_005274273.1:p.Gln248His
XM_005274218.3:c.606G>T	XP_005274275.1:p.Gln202His
XM_005274219.2:c.867+57G>T	XP_005274276.1:n.867+57G>T
XM_005274221.2:c.714+891G>T	XP_005274278.1:n.714+891G>T
XM_011545229.1:c.867+57G>T	XP_011543531.1:n.867+57G>T
XM_011545230.1:c.774+57G>T	XP_011543532.1:n.774+57G>T
XM_011545231.1:c.549+57G>T	XP_011543533.1:n.549+57G>T
XM_011545232.1:c.924G>T	XP_011543534.1:p.Gln308His
NM_001363591.1:c.549+57G>T	NP_001350520.1:n.549+57G>T
NM_001363592.1:c.924G>T	NP_001350521.1:p.Gln308His
NM_001363593.1:c.-252G>T	NP_001350522.1:n.-252G>T
NR_134580.1:n.1504G>T
XM_005274210.4:c.867+57G>T	XP_005274267.1:n.867+57G>T
XM_005274215.4:c.549+57G>T	XP_005274272.1:n.549+57G>T
XM_005274216.4:c.744G>T	XP_005274273.1:p.Gln248His
XM_005274219.4:c.867+57G>T	XP_005274276.1:n.867+57G>T
XM_005274221.4:c.714+891G>T	XP_005274278.1:n.714+891G>T
XM_011545229.3:c.867+57G>T	XP_011543531.1:n.867+57G>T
XM_011545230.3:c.774+57G>T	XP_011543532.1:n.774+57G>T
XM_017018230.2:c.606G>T	XP_016873719.1:p.Gln202His
XR_001747952.2:n.1422G>T
XR_001747953.2:n.1557+57G>T
XR_001747954.2:n.1404+891G>T
XR_001748245.1:n.374C>A
XR_002957249.1:n.374C>A
NM_004183.4:c.867+57G>T MANE Select	NP_004174.1:n.867+57G>T
NM_001139443.2:c.687+57G>T	NP_001132915.1:n.687+57G>T
NM_001300786.2:c.687+57G>T	NP_001287715.1:n.687+57G>T
NM_001300787.2:c.687+57G>T	NP_001287716.1:n.687+57G>T
NM_001363591.2:c.549+57G>T	NP_001350520.1:n.549+57G>T
NM_001363593.2:c.-252G>T	NP_001350522.1:n.-252G>T
NR_134580.2:n.1037G>T