Canonical Allele Identifier: CA380835249

Gene: BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61723370T>A (hg19) ; chr11:g.61955898T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61955898T>A , CM000673.2:g.61955898T>A	GRCh38
NC_000011.9:g.61723370T>A , CM000673.1:g.61723370T>A	GRCh37
NC_000011.8:g.61479946T>A	NCBI36
NG_009033.1:g.11015T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378043.9:c.428T>A MANE Select	ENSP00000367282.4:p.Val143Asp
ENST00000378043.8:c.428T>A	ENSP00000367282.4:p.Val143Asp
ENST00000449131.6:c.248T>A	ENSP00000399709.2:p.Val83Asp
ENST00000524877.5:n.860T>A
ENST00000524926.5:c.428T>A	ENSP00000432681.1:p.Val143Asp
ENST00000526988.1:c.110T>A	ENSP00000433195.1:p.Val37Asp
ENST00000529265.5:n.351T>A
ENST00000533521.5:n.1052T>A
ENST00000534553.5:c.110T>A	ENSP00000431189.1:p.Val37Asp
NM_001139443.1:c.248T>A	NP_001132915.1:p.Val83Asp
NM_001300786.1:c.248T>A	NP_001287715.1:p.Val83Asp
NM_001300787.1:c.248T>A	NP_001287716.1:p.Val83Asp
NM_004183.3:c.428T>A	NP_004174.1:p.Val143Asp
XM_005274210.2:c.428T>A	XP_005274267.1:p.Val143Asp
XM_005274215.2:c.110T>A	XP_005274272.1:p.Val37Asp
XM_005274216.2:c.248T>A	XP_005274273.1:p.Val83Asp
XM_005274218.3:c.110T>A	XP_005274275.1:p.Val37Asp
XM_005274219.2:c.428T>A	XP_005274276.1:p.Val143Asp
XM_005274221.2:c.428T>A	XP_005274278.1:p.Val143Asp
XM_011545229.1:c.428T>A	XP_011543531.1:p.Val143Asp
XM_011545230.1:c.335T>A	XP_011543532.1:p.Val112Asp
XM_011545231.1:c.110T>A	XP_011543533.1:p.Val37Asp
XM_011545232.1:c.428T>A	XP_011543534.1:p.Val143Asp
NM_001363591.1:c.110T>A	NP_001350520.1:p.Val37Asp
NM_001363592.1:c.428T>A	NP_001350521.1:p.Val143Asp
NM_001363593.1:c.-748T>A	NP_001350522.1:n.-748T>A
NR_134580.1:n.1008T>A
XM_005274210.4:c.428T>A	XP_005274267.1:p.Val143Asp
XM_005274215.4:c.110T>A	XP_005274272.1:p.Val37Asp
XM_005274216.4:c.248T>A	XP_005274273.1:p.Val83Asp
XM_005274219.4:c.428T>A	XP_005274276.1:p.Val143Asp
XM_005274221.4:c.428T>A	XP_005274278.1:p.Val143Asp
XM_011545229.3:c.428T>A	XP_011543531.1:p.Val143Asp
XM_011545230.3:c.335T>A	XP_011543532.1:p.Val112Asp
XM_017018230.2:c.110T>A	XP_016873719.1:p.Val37Asp
XR_001747952.2:n.926T>A
XR_001747953.2:n.1118T>A
XR_001747954.2:n.1118T>A
XR_002957249.1:n.1840A>T
NM_004183.4:c.428T>A MANE Select	NP_004174.1:p.Val143Asp
NM_001139443.2:c.248T>A	NP_001132915.1:p.Val83Asp
NM_001300786.2:c.248T>A	NP_001287715.1:p.Val83Asp
NM_001300787.2:c.248T>A	NP_001287716.1:p.Val83Asp
NM_001363591.2:c.110T>A	NP_001350520.1:p.Val37Asp
NM_001363593.2:c.-748T>A	NP_001350522.1:n.-748T>A
NR_134580.2:n.541T>A