Canonical Allele Identifier: CA6040863

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61958253C>T , CM000673.2:g.61958253C>T	GRCh38
NC_000011.9:g.61725725C>T , CM000673.1:g.61725725C>T	GRCh37
NC_000011.8:g.61482301C>T	NCBI36
NG_009033.1:g.13370C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004183.4:c.822C>T MANE Select	NP_004174.1:p.Pro274=
ENST00000378043.9:c.822C>T MANE Select	ENSP00000367282.4:p.Pro274=
NM_001139443.1:c.642C>T	NP_001132915.1:p.Pro214=
NM_001139443.2:c.642C>T	NP_001132915.1:p.Pro214=
NM_001300786.1:c.642C>T	NP_001287715.1:p.Pro214=
NM_001300786.2:c.642C>T	NP_001287715.1:p.Pro214=
NM_001300787.1:c.642C>T	NP_001287716.1:p.Pro214=
NM_001300787.2:c.642C>T	NP_001287716.1:p.Pro214=
NM_001363591.1:c.504C>T	NP_001350520.1:p.Pro168=
NM_001363591.2:c.504C>T	NP_001350520.1:p.Pro168=
NM_001363592.1:c.822C>T	NP_001350521.1:p.Pro274=
NM_001363593.1:c.-354C>T	NP_001350522.1:n.-354C>T
NM_001363593.2:c.-354C>T	NP_001350522.1:n.-354C>T
NM_004183.3:c.822C>T	NP_004174.1:p.Pro274=
NR_134580.1:n.1402C>T
NR_134580.2:n.935C>T
ENST00000378043.8:c.822C>T	ENSP00000367282.4:p.Pro274=
ENST00000449131.6:c.642C>T	ENSP00000399709.2:p.Pro214=
ENST00000524877.5:n.1254C>T
ENST00000524926.5:c.822C>T	ENSP00000432681.1:p.Pro274=
ENST00000526988.1:c.504C>T	ENSP00000433195.1:p.Pro168=
ENST00000529265.5:n.745C>T
ENST00000534553.5:c.163+2302C>T	ENSP00000431189.1:n.163+2302C>T
XM_005274210.2:c.822C>T	XP_005274267.1:p.Pro274=
XM_005274210.4:c.822C>T	XP_005274267.1:p.Pro274=
XM_005274215.2:c.504C>T	XP_005274272.1:p.Pro168=
XM_005274215.4:c.504C>T	XP_005274272.1:p.Pro168=
XM_005274216.2:c.642C>T	XP_005274273.1:p.Pro214=
XM_005274216.4:c.642C>T	XP_005274273.1:p.Pro214=
XM_005274218.3:c.504C>T	XP_005274275.1:p.Pro168=
XM_005274219.2:c.822C>T	XP_005274276.1:p.Pro274=
XM_005274219.4:c.822C>T	XP_005274276.1:p.Pro274=
XM_005274221.2:c.714+789C>T	XP_005274278.1:n.714+789C>T
XM_005274221.4:c.714+789C>T	XP_005274278.1:n.714+789C>T
XM_011545229.1:c.822C>T	XP_011543531.1:p.Pro274=
XM_011545229.3:c.822C>T	XP_011543531.1:p.Pro274=
XM_011545230.1:c.729C>T	XP_011543532.1:p.Pro243=
XM_011545230.3:c.729C>T	XP_011543532.1:p.Pro243=
XM_011545231.1:c.504C>T	XP_011543533.1:p.Pro168=
XM_011545232.1:c.822C>T	XP_011543534.1:p.Pro274=
XM_017018230.2:c.504C>T	XP_016873719.1:p.Pro168=
XR_001747952.2:n.1320C>T
XR_001747953.2:n.1512C>T
XR_001747954.2:n.1404+789C>T
XR_001748245.1:n.476G>A
XR_002957249.1:n.476G>A