Canonical Allele Identifier: CA7703826

Gene: BNC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.83262978G>A , CM000677.2:g.83262978G>A	GRCh38
NC_000015.9:g.83931730G>A , CM000677.1:g.83931730G>A	GRCh37
NC_000015.8:g.81722734G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001717.4:c.2273C>T MANE Select	NP_001708.3:p.Thr758Ile
ENST00000345382.7:c.2273C>T MANE Select	ENSP00000307041.2:p.Thr758Ile
NM_001301206.1:c.2252C>T	NP_001288135.1:p.Thr751Ile
NM_001301206.2:c.2252C>T	NP_001288135.1:p.Thr751Ile
NM_001717.3:c.2273C>T	NP_001708.3:p.Thr758Ile
ENST00000345382.6:c.2273C>T	ENSP00000307041.2:p.Thr758Ile
ENST00000569704.1:c.2252C>T	ENSP00000456727.1:p.Thr751Ile
ENST00000569704.2:c.2252C>T	ENSP00000456727.1:p.Thr751Ile
ENST00000618086.4:c.2270C>T	ENSP00000478817.1:p.Thr757Ile
XM_011521893.1:c.2198C>T	XP_011520195.1:p.Thr733Ile
XM_011521894.1:c.1919C>T	XP_011520196.1:p.Thr640Ile