Canonical Allele Identifier: CA1977558531

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61950210G= , CM000673.2:g.61950210G=	GRCh38
NC_000011.9:g.61717682G= , CM000673.1:g.61717682G=	GRCh37
NC_000011.8:g.61474258G=	NCBI36
NG_009033.1:g.5327G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.8:c.-254G=	ENSP00000367282.4:n.-254G=
ENST00000534553.5:c.-429G=	ENSP00000431189.1:n.-429G=
NM_001139443.1:c.-246G=	NP_001132915.1:n.-246G=
NM_001300786.1:c.-246G=	NP_001287715.1:n.-246G=
NM_001300787.1:c.-246G=	NP_001287716.1:n.-246G=
NM_004183.3:c.-254G=	NP_004174.1:n.-254G=
XM_005274210.2:c.-254G=	XP_005274267.1:n.-254G=
XM_005274216.2:c.-246G=	XP_005274273.1:n.-246G=
XM_005274218.3:c.-429G=	XP_005274275.1:n.-429G=
XM_005274219.2:c.-254G=	XP_005274276.1:n.-254G=
XM_005274221.2:c.-254G=	XP_005274278.1:n.-254G=
XM_011545229.1:c.-36-1561G=	XP_011543531.1:n.-36-1561G=
XM_011545230.1:c.59+3395G=	XP_011543532.1:n.59+3395G=
XM_011545231.1:c.-429G=	XP_011543533.1:n.-429G=
XM_011545232.1:c.-254G=	XP_011543534.1:n.-254G=
NM_001363592.1:c.-254G=	NP_001350521.1:n.-254G=
NR_134580.1:n.327G=
XM_005274210.4:c.-254G=	XP_005274267.1:n.-254G=
XM_005274216.4:c.-246G=	XP_005274273.1:n.-246G=
XM_005274219.4:c.-254G=	XP_005274276.1:n.-254G=
XM_005274221.4:c.-254G=	XP_005274278.1:n.-254G=
XM_011545229.3:c.-36-1561G=	XP_011543531.1:n.-36-1561G=
XM_011545230.3:c.59+3395G=	XP_011543532.1:n.59+3395G=
XR_001747952.2:n.433G=
XR_001747953.2:n.437G=
XR_001747954.2:n.437G=