Canonical Allele Identifier: CA2613924442

Gene: BEST1

Linked Data

• gnomAD v4: 11-61955687-TCGCCCCTCGCCCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61955696_61955709del , CM000673.2:g.61955696_61955709del	GRCh38
NC_000011.9:g.61723168_61723181del , CM000673.1:g.61723168_61723181del	GRCh37
NC_000011.8:g.61479744_61479757del	NCBI36
NG_009033.1:g.10813_10826del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378043.9:c.248-22_248-9del MANE Select	ENSP00000367282.4:n.248-22_248-9del
ENST00000378043.8:c.248-22_248-9del	ENSP00000367282.4:n.248-22_248-9del
ENST00000449131.6:c.68-22_68-9del	ENSP00000399709.2:n.68-22_68-9del
ENST00000524877.5:n.658_671del
ENST00000524926.5:c.248-22_248-9del	ENSP00000432681.1:n.248-22_248-9del
ENST00000526988.1:c.-71-22_-71-9del	ENSP00000433195.1:n.-71-22_-71-9del
ENST00000529265.5:n.171-22_171-9del
ENST00000533521.5:n.850_863del
ENST00000534553.5:c.-71-22_-71-9del	ENSP00000431189.1:n.-71-22_-71-9del
NM_001139443.1:c.68-22_68-9del	NP_001132915.1:n.68-22_68-9del
NM_001300786.1:c.68-22_68-9del	NP_001287715.1:n.68-22_68-9del
NM_001300787.1:c.68-22_68-9del	NP_001287716.1:n.68-22_68-9del
NM_004183.3:c.248-22_248-9del	NP_004174.1:n.248-22_248-9del
XM_005274210.2:c.248-22_248-9del	XP_005274267.1:n.248-22_248-9del
XM_005274215.2:c.-71-22_-71-9del	XP_005274272.1:n.-71-22_-71-9del
XM_005274216.2:c.68-22_68-9del	XP_005274273.1:n.68-22_68-9del
XM_005274218.3:c.-71-22_-71-9del	XP_005274275.1:n.-71-22_-71-9del
XM_005274219.2:c.248-22_248-9del	XP_005274276.1:n.248-22_248-9del
XM_005274221.2:c.248-22_248-9del	XP_005274278.1:n.248-22_248-9del
XM_011545229.1:c.248-22_248-9del	XP_011543531.1:n.248-22_248-9del
XM_011545230.1:c.155-22_155-9del	XP_011543532.1:n.155-22_155-9del
XM_011545231.1:c.-71-22_-71-9del	XP_011543533.1:n.-71-22_-71-9del
XM_011545232.1:c.248-22_248-9del	XP_011543534.1:n.248-22_248-9del
NM_001363591.1:c.-71-22_-71-9del	NP_001350520.1:n.-71-22_-71-9del
NM_001363592.1:c.248-22_248-9del	NP_001350521.1:n.248-22_248-9del
NM_001363593.1:c.-928-22_-928-9del	NP_001350522.1:n.-928-22_-928-9del
NR_134580.1:n.828-22_828-9del
XM_005274210.4:c.248-22_248-9del	XP_005274267.1:n.248-22_248-9del
XM_005274215.4:c.-71-22_-71-9del	XP_005274272.1:n.-71-22_-71-9del
XM_005274216.4:c.68-22_68-9del	XP_005274273.1:n.68-22_68-9del
XM_005274219.4:c.248-22_248-9del	XP_005274276.1:n.248-22_248-9del
XM_005274221.4:c.248-22_248-9del	XP_005274278.1:n.248-22_248-9del
XM_011545229.3:c.248-22_248-9del	XP_011543531.1:n.248-22_248-9del
XM_011545230.3:c.155-22_155-9del	XP_011543532.1:n.155-22_155-9del
XM_017018230.2:c.-71-22_-71-9del	XP_016873719.1:n.-71-22_-71-9del
XR_001747952.2:n.746-22_746-9del
XR_001747953.2:n.938-22_938-9del
XR_001747954.2:n.938-22_938-9del
XR_002957249.1:n.2037_2050del
NM_004183.4:c.248-22_248-9del MANE Select	NP_004174.1:n.248-22_248-9del
NM_001139443.2:c.68-22_68-9del	NP_001132915.1:n.68-22_68-9del
NM_001300786.2:c.68-22_68-9del	NP_001287715.1:n.68-22_68-9del
NM_001300787.2:c.68-22_68-9del	NP_001287716.1:n.68-22_68-9del
NM_001363591.2:c.-71-22_-71-9del	NP_001350520.1:n.-71-22_-71-9del
NM_001363593.2:c.-928-22_-928-9del	NP_001350522.1:n.-928-22_-928-9del
NR_134580.2:n.361-22_361-9del