Canonical Allele Identifier: CA2792344335

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61950485_61950486insCT , CM000673.2:g.61950485_61950486insCT	GRCh38
NC_000011.9:g.61717957_61717958insCT , CM000673.1:g.61717957_61717958insCT	GRCh37
NC_000011.8:g.61474533_61474534insCT	NCBI36
NG_009033.1:g.5602_5603insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.-37+58_-37+59insCT MANE Select	ENSP00000367282.4:n.-37+58_-37+59insCT
ENST00000378043.8:c.-37+58_-37+59insCT	ENSP00000367282.4:n.-37+58_-37+59insCT
ENST00000449131.6:c.-29+58_-29+59insCT	ENSP00000399709.2:n.-29+58_-29+59insCT
ENST00000524877.5:n.68+58_68+59insCT
ENST00000524926.5:c.-37+58_-37+59insCT	ENSP00000432681.1:n.-37+58_-37+59insCT
ENST00000529265.5:n.75+58_75+59insCT
ENST00000533521.5:n.72+58_72+59insCT
ENST00000534553.5:c.-212+58_-212+59insCT	ENSP00000431189.1:n.-212+58_-212+59insCT
NM_001139443.1:c.-29+58_-29+59insCT	NP_001132915.1:n.-29+58_-29+59insCT
NM_001300786.1:c.-29+58_-29+59insCT	NP_001287715.1:n.-29+58_-29+59insCT
NM_001300787.1:c.-29+58_-29+59insCT	NP_001287716.1:n.-29+58_-29+59insCT
NM_004183.3:c.-37+58_-37+59insCT	NP_004174.1:n.-37+58_-37+59insCT
XM_005274210.2:c.-37+58_-37+59insCT	XP_005274267.1:n.-37+58_-37+59insCT
XM_005274216.2:c.-29+58_-29+59insCT	XP_005274273.1:n.-29+58_-29+59insCT
XM_005274218.3:c.-212+58_-212+59insCT	XP_005274275.1:n.-212+58_-212+59insCT
XM_005274219.2:c.-37+58_-37+59insCT	XP_005274276.1:n.-37+58_-37+59insCT
XM_005274221.2:c.-37+58_-37+59insCT	XP_005274278.1:n.-37+58_-37+59insCT
XM_011545229.1:c.-36-1286_-36-1285insCT	XP_011543531.1:n.-36-1286_-36-1285insCT
XM_011545230.1:c.59+3670_59+3671insCT	XP_011543532.1:n.59+3670_59+3671insCT
XM_011545231.1:c.-212+58_-212+59insCT	XP_011543533.1:n.-212+58_-212+59insCT
XM_011545232.1:c.-37+58_-37+59insCT	XP_011543534.1:n.-37+58_-37+59insCT
NM_001363592.1:c.-37+58_-37+59insCT	NP_001350521.1:n.-37+58_-37+59insCT
NR_134580.1:n.544+58_544+59insCT
XM_005274210.4:c.-37+58_-37+59insCT	XP_005274267.1:n.-37+58_-37+59insCT
XM_005274216.4:c.-29+58_-29+59insCT	XP_005274273.1:n.-29+58_-29+59insCT
XM_005274219.4:c.-37+58_-37+59insCT	XP_005274276.1:n.-37+58_-37+59insCT
XM_005274221.4:c.-37+58_-37+59insCT	XP_005274278.1:n.-37+58_-37+59insCT
XM_011545229.3:c.-36-1286_-36-1285insCT	XP_011543531.1:n.-36-1286_-36-1285insCT
XM_011545230.3:c.59+3670_59+3671insCT	XP_011543532.1:n.59+3670_59+3671insCT
XR_001747952.2:n.650+58_650+59insCT
XR_001747953.2:n.654+58_654+59insCT
XR_001747954.2:n.654+58_654+59insCT
NM_004183.4:c.-37+58_-37+59insCT MANE Select	NP_004174.1:n.-37+58_-37+59insCT
NM_001139443.2:c.-29+58_-29+59insCT	NP_001132915.1:n.-29+58_-29+59insCT
NM_001300786.2:c.-29+58_-29+59insCT	NP_001287715.1:n.-29+58_-29+59insCT
NM_001300787.2:c.-29+58_-29+59insCT	NP_001287716.1:n.-29+58_-29+59insCT
NR_134580.2:n.77+58_77+59insCT