Canonical Allele Identifier: CA1977558630

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61950431A= , CM000673.2:g.61950431A=	GRCh38
NC_000011.9:g.61717903A= , CM000673.1:g.61717903A=	GRCh37
NC_000011.8:g.61474479A=	NCBI36
NG_009033.1:g.5548A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.-37+4A= MANE Select	ENSP00000367282.4:n.-37+4A=
ENST00000378043.8:c.-37+4A=	ENSP00000367282.4:n.-37+4A=
ENST00000449131.6:c.-29+4A=	ENSP00000399709.2:n.-29+4A=
ENST00000524877.5:n.68+4A=
ENST00000524926.5:c.-37+4A=	ENSP00000432681.1:n.-37+4A=
ENST00000529265.5:n.75+4A=
ENST00000533521.5:n.72+4A=
ENST00000534553.5:c.-212+4A=	ENSP00000431189.1:n.-212+4A=
NM_001139443.1:c.-29+4A=	NP_001132915.1:n.-29+4A=
NM_001300786.1:c.-29+4A=	NP_001287715.1:n.-29+4A=
NM_001300787.1:c.-29+4A=	NP_001287716.1:n.-29+4A=
NM_004183.3:c.-37+4A=	NP_004174.1:n.-37+4A=
XM_005274210.2:c.-37+4A=	XP_005274267.1:n.-37+4A=
XM_005274216.2:c.-29+4A=	XP_005274273.1:n.-29+4A=
XM_005274218.3:c.-212+4A=	XP_005274275.1:n.-212+4A=
XM_005274219.2:c.-37+4A=	XP_005274276.1:n.-37+4A=
XM_005274221.2:c.-37+4A=	XP_005274278.1:n.-37+4A=
XM_011545229.1:c.-36-1340A=	XP_011543531.1:n.-36-1340A=
XM_011545230.1:c.59+3616A=	XP_011543532.1:n.59+3616A=
XM_011545231.1:c.-212+4A=	XP_011543533.1:n.-212+4A=
XM_011545232.1:c.-37+4A=	XP_011543534.1:n.-37+4A=
NM_001363592.1:c.-37+4A=	NP_001350521.1:n.-37+4A=
NR_134580.1:n.544+4A=
XM_005274210.4:c.-37+4A=	XP_005274267.1:n.-37+4A=
XM_005274216.4:c.-29+4A=	XP_005274273.1:n.-29+4A=
XM_005274219.4:c.-37+4A=	XP_005274276.1:n.-37+4A=
XM_005274221.4:c.-37+4A=	XP_005274278.1:n.-37+4A=
XM_011545229.3:c.-36-1340A=	XP_011543531.1:n.-36-1340A=
XM_011545230.3:c.59+3616A=	XP_011543532.1:n.59+3616A=
XR_001747952.2:n.650+4A=
XR_001747953.2:n.654+4A=
XR_001747954.2:n.654+4A=
NM_004183.4:c.-37+4A= MANE Select	NP_004174.1:n.-37+4A=
NM_001139443.2:c.-29+4A=	NP_001132915.1:n.-29+4A=
NM_001300786.2:c.-29+4A=	NP_001287715.1:n.-29+4A=
NM_001300787.2:c.-29+4A=	NP_001287716.1:n.-29+4A=
NR_134580.2:n.77+4A=