Canonical Allele Identifier: CA4995928

Gene: BNC2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.16435921C>T , CM000671.2:g.16435921C>T	GRCh38
NC_000009.11:g.16435919C>T , CM000671.1:g.16435919C>T	GRCh37
NC_000009.10:g.16425919C>T	NCBI36
NG_051226.1:g.439918G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_017637.6:c.2273G>A MANE Select	NP_060107.3:p.Arg758Lys
ENST00000380672.9:c.2273G>A MANE Select	ENSP00000370047.3:p.Arg758Lys
NM_001317939.1:c.2147G>A	NP_001304868.1:p.Arg716Lys
NM_001317939.2:c.2147G>A	NP_001304868.1:p.Arg716Lys
NM_001317940.1:c.1988G>A	NP_001304869.1:p.Arg663Lys
NM_001317940.2:c.1988G>A	NP_001304869.1:p.Arg663Lys
NM_017637.5:c.2273G>A	NP_060107.3:p.Arg758Lys
ENST00000380667.6:c.2072G>A	ENSP00000370042.1:p.Arg691Lys
ENST00000380672.8:c.2273G>A	ENSP00000370047.3:p.Arg758Lys
ENST00000411752.5:c.452G>A	ENSP00000392212.1:p.Arg151Lys
ENST00000418777.5:c.2144G>A	ENSP00000408370.1:p.Arg715Lys
ENST00000484726.5:c.2273G>A	ENSP00000431516.1:p.Arg758Lys
ENST00000545497.5:c.1751G>A	ENSP00000444640.2:p.Arg584Lys
ENST00000700553.1:c.1943G>A	ENSP00000515060.1:p.Arg648Lys
XM_011517921.1:c.2357G>A	XP_011516223.1:p.Arg786Lys
XM_011517922.1:c.2315G>A	XP_011516224.1:p.Arg772Lys
XM_011517923.1:c.2315G>A	XP_011516225.1:p.Arg772Lys
XM_011517924.1:c.2147G>A	XP_011516226.1:p.Arg716Lys
XM_011517924.2:c.2147G>A	XP_011516226.1:p.Arg716Lys
XM_011517925.1:c.1976G>A	XP_011516227.1:p.Arg659Lys
XM_011517926.1:c.1946G>A	XP_011516228.1:p.Arg649Lys
XM_011517927.1:c.1751G>A	XP_011516229.1:p.Arg584Lys
XM_011517928.1:c.2399G>A	XP_011516230.1:p.Arg800Lys
XM_011517929.1:c.1568G>A	XP_011516231.1:p.Arg523Lys
XM_011517930.1:c.1568G>A	XP_011516232.1:p.Arg523Lys
XM_011517931.1:c.1568G>A	XP_011516233.1:p.Arg523Lys
XM_011517932.1:c.1568G>A	XP_011516234.1:p.Arg523Lys
XM_011517933.1:c.2147G>A	XP_011516235.1:p.Arg716Lys
XM_011517934.1:c.1751G>A	XP_011516236.1:p.Arg584Lys
XM_011517934.2:c.1751G>A	XP_011516236.1:p.Arg584Lys
XM_017014816.1:c.2399G>A	XP_016870305.1:p.Arg800Lys
XM_017014817.1:c.2399G>A	XP_016870306.1:p.Arg800Lys
XM_017014818.1:c.2315G>A	XP_016870307.1:p.Arg772Lys
XM_017014819.1:c.2399G>A	XP_016870308.1:p.Arg800Lys
XM_017014820.1:c.2399G>A	XP_016870309.1:p.Arg800Lys
XM_017014821.1:c.2315G>A	XP_016870310.1:p.Arg772Lys
XM_017014822.1:c.1946G>A	XP_016870311.1:p.Arg649Lys
XM_017014823.1:c.1946G>A	XP_016870312.1:p.Arg649Lys
XM_017014824.1:c.1751G>A	XP_016870313.1:p.Arg584Lys
XM_017014825.2:c.2399G>A	XP_016870314.1:p.Arg800Lys
XM_017014826.1:c.2399G>A	XP_016870315.1:p.Arg800Lys
XM_017014827.1:c.2399G>A	XP_016870316.1:p.Arg800Lys
XM_017014828.1:c.2399G>A	XP_016870317.1:p.Arg800Lys
XM_017014829.2:c.1568G>A	XP_016870318.1:p.Arg523Lys