Canonical Allele Identifier: CA2792344318

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61950204_61950205insGGC , CM000673.2:g.61950204_61950205insGGC	GRCh38
NC_000011.9:g.61717676_61717677insGGC , CM000673.1:g.61717676_61717677insGGC	GRCh37
NC_000011.8:g.61474252_61474253insGGC	NCBI36
NG_009033.1:g.5321_5322insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.8:c.-260_-259insGGC	ENSP00000367282.4:n.-260_-259insGGC
ENST00000534553.5:c.-435_-434insGGC	ENSP00000431189.1:n.-435_-434insGGC
NM_001139443.1:c.-252_-251insGGC	NP_001132915.1:n.-252_-251insGGC
NM_001300786.1:c.-252_-251insGGC	NP_001287715.1:n.-252_-251insGGC
NM_001300787.1:c.-252_-251insGGC	NP_001287716.1:n.-252_-251insGGC
NM_004183.3:c.-260_-259insGGC	NP_004174.1:n.-260_-259insGGC
XM_005274210.2:c.-260_-259insGGC	XP_005274267.1:n.-260_-259insGGC
XM_005274216.2:c.-252_-251insGGC	XP_005274273.1:n.-252_-251insGGC
XM_005274218.3:c.-435_-434insGGC	XP_005274275.1:n.-435_-434insGGC
XM_005274219.2:c.-260_-259insGGC	XP_005274276.1:n.-260_-259insGGC
XM_005274221.2:c.-260_-259insGGC	XP_005274278.1:n.-260_-259insGGC
XM_011545229.1:c.-36-1567_-36-1566insGGC	XP_011543531.1:n.-36-1567_-36-1566insGGC
XM_011545230.1:c.59+3389_59+3390insGGC	XP_011543532.1:n.59+3389_59+3390insGGC
XM_011545231.1:c.-435_-434insGGC	XP_011543533.1:n.-435_-434insGGC
XM_011545232.1:c.-260_-259insGGC	XP_011543534.1:n.-260_-259insGGC
NM_001363592.1:c.-260_-259insGGC	NP_001350521.1:n.-260_-259insGGC
NR_134580.1:n.321_322insGGC
XM_005274210.4:c.-260_-259insGGC	XP_005274267.1:n.-260_-259insGGC
XM_005274216.4:c.-252_-251insGGC	XP_005274273.1:n.-252_-251insGGC
XM_005274219.4:c.-260_-259insGGC	XP_005274276.1:n.-260_-259insGGC
XM_005274221.4:c.-260_-259insGGC	XP_005274278.1:n.-260_-259insGGC
XM_011545229.3:c.-36-1567_-36-1566insGGC	XP_011543531.1:n.-36-1567_-36-1566insGGC
XM_011545230.3:c.59+3389_59+3390insGGC	XP_011543532.1:n.59+3389_59+3390insGGC
XR_001747952.2:n.427_428insGGC
XR_001747953.2:n.431_432insGGC
XR_001747954.2:n.431_432insGGC