Canonical Allele Identifier: CA11639059

Gene: BST1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15735725G>A , CM000666.2:g.15735725G>A	GRCh38
NC_000004.11:g.15737348G>A , CM000666.1:g.15737348G>A	GRCh37
NC_000004.10:g.15346446G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000514445.5:c.402-328G>A	ENSP00000420925.1:n.402-328G>A
ENST00000514989.1:c.275-2062G>A
XM_005248184.3:c.852-328G>A	XP_005248241.1:n.852-328G>A
XM_005248186.1:c.852-2062G>A	XP_005248243.1:n.852-2062G>A
XM_011513878.1:c.851+12791G>A	XP_011512180.1:n.851+12791G>A
XM_011513879.1:c.852-1983G>A	XP_011512181.1:n.852-1983G>A
XM_005248186.2:c.852-2062G>A	XP_005248243.1:n.852-2062G>A
XM_011513878.3:c.851+12791G>A	XP_011512180.1:n.851+12791G>A
XM_011513879.2:c.852-1983G>A	XP_011512181.1:n.852-1983G>A
XM_017008565.2:c.852-328G>A	XP_016864054.1:n.852-328G>A
XM_017008566.2:c.851+12791G>A	XP_016864055.1:n.851+12791G>A