Canonical Allele Identifier: CA1440782081

Gene: BST1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15727911G= , CM000666.2:g.15727911G=	GRCh38
NC_000004.11:g.15729534G= , CM000666.1:g.15729534G=	GRCh37
NC_000004.10:g.15338632G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265016.9:c.852-3829G= MANE Select	ENSP00000265016.4:n.852-3829G=
ENST00000265016.8:c.852-3829G=	ENSP00000265016.4:n.852-3829G=
ENST00000382346.7:c.897-3829G=	ENSP00000371783.3:n.897-3829G=
ENST00000514445.5:c.401+4977G=	ENSP00000420925.1:n.401+4977G=
ENST00000514989.1:c.274+4977G=
NM_004334.2:c.852-3829G=	NP_004325.2:n.852-3829G=
XM_005248184.3:c.851+4977G=	XP_005248241.1:n.851+4977G=
XM_005248186.1:c.851+4977G=	XP_005248243.1:n.851+4977G=
XM_011513878.1:c.851+4977G=	XP_011512180.1:n.851+4977G=
XM_011513879.1:c.851+4977G=	XP_011512181.1:n.851+4977G=
XM_011513880.1:c.852-2723G=	XP_011512182.1:n.852-2723G=
XM_011513881.1:c.678-3829G=	XP_011512183.1:n.678-3829G=
XM_005248186.2:c.851+4977G=	XP_005248243.1:n.851+4977G=
XM_011513878.3:c.851+4977G=	XP_011512180.1:n.851+4977G=
XM_011513879.2:c.851+4977G=	XP_011512181.1:n.851+4977G=
XM_011513881.2:c.678-3829G=	XP_011512183.1:n.678-3829G=
XM_017008565.2:c.851+4977G=	XP_016864054.1:n.851+4977G=
XM_017008566.2:c.851+4977G=	XP_016864055.1:n.851+4977G=
NM_004334.3:c.852-3829G= MANE Select	NP_004325.2:n.852-3829G=