Canonical Allele Identifier: CA1977558597

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61950363G= , CM000673.2:g.61950363G=	GRCh38
NC_000011.9:g.61717835G= , CM000673.1:g.61717835G=	GRCh37
NC_000011.8:g.61474411G=	NCBI36
NG_009033.1:g.5480G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.-101G= MANE Select	ENSP00000367282.4:n.-101G=
ENST00000378043.8:c.-101G=	ENSP00000367282.4:n.-101G=
ENST00000524877.5:n.4G=
ENST00000524926.5:c.-101G=	ENSP00000432681.1:n.-101G=
ENST00000529265.5:n.11G=
ENST00000533521.5:n.8G=
ENST00000534553.5:c.-276G=	ENSP00000431189.1:n.-276G=
NM_001139443.1:c.-93G=	NP_001132915.1:n.-93G=
NM_001300786.1:c.-93G=	NP_001287715.1:n.-93G=
NM_001300787.1:c.-93G=	NP_001287716.1:n.-93G=
NM_004183.3:c.-101G=	NP_004174.1:n.-101G=
XM_005274210.2:c.-101G=	XP_005274267.1:n.-101G=
XM_005274216.2:c.-93G=	XP_005274273.1:n.-93G=
XM_005274218.3:c.-276G=	XP_005274275.1:n.-276G=
XM_005274219.2:c.-101G=	XP_005274276.1:n.-101G=
XM_005274221.2:c.-101G=	XP_005274278.1:n.-101G=
XM_011545229.1:c.-36-1408G=	XP_011543531.1:n.-36-1408G=
XM_011545230.1:c.59+3548G=	XP_011543532.1:n.59+3548G=
XM_011545231.1:c.-276G=	XP_011543533.1:n.-276G=
XM_011545232.1:c.-101G=	XP_011543534.1:n.-101G=
NM_001363592.1:c.-101G=	NP_001350521.1:n.-101G=
NR_134580.1:n.480G=
XM_005274210.4:c.-101G=	XP_005274267.1:n.-101G=
XM_005274216.4:c.-93G=	XP_005274273.1:n.-93G=
XM_005274219.4:c.-101G=	XP_005274276.1:n.-101G=
XM_005274221.4:c.-101G=	XP_005274278.1:n.-101G=
XM_011545229.3:c.-36-1408G=	XP_011543531.1:n.-36-1408G=
XM_011545230.3:c.59+3548G=	XP_011543532.1:n.59+3548G=
XR_001747952.2:n.586G=
XR_001747953.2:n.590G=
XR_001747954.2:n.590G=
NM_004183.4:c.-101G= MANE Select	NP_004174.1:n.-101G=
NM_001139443.2:c.-93G=	NP_001132915.1:n.-93G=
NM_001300786.2:c.-93G=	NP_001287715.1:n.-93G=
NM_001300787.2:c.-93G=	NP_001287716.1:n.-93G=
NR_134580.2:n.13G=