Canonical Allele Identifier: CA204330

Gene: BNC2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.16435716T>C , CM000671.2:g.16435716T>C	GRCh38
NC_000009.11:g.16435714T>C , CM000671.1:g.16435714T>C	GRCh37
NC_000009.10:g.16425714T>C	NCBI36
NG_051226.1:g.440123A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_017637.6:c.2478A>G MANE Select	NP_060107.3:p.Leu826=
ENST00000380672.9:c.2478A>G MANE Select	ENSP00000370047.3:p.Leu826=
NM_001317939.1:c.2352A>G	NP_001304868.1:p.Leu784=
NM_001317939.2:c.2352A>G	NP_001304868.1:p.Leu784=
NM_001317940.1:c.2193A>G	NP_001304869.1:p.Leu731=
NM_001317940.2:c.2193A>G	NP_001304869.1:p.Leu731=
NM_017637.5:c.2478A>G	NP_060107.3:p.Leu826=
ENST00000380667.6:c.2277A>G	ENSP00000370042.1:p.Leu759=
ENST00000380672.8:c.2478A>G	ENSP00000370047.3:p.Leu826=
ENST00000411752.5:c.657A>G	ENSP00000392212.1:p.Leu219=
ENST00000418777.5:c.2349A>G	ENSP00000408370.1:p.Leu783=
ENST00000484726.5:c.2478A>G	ENSP00000431516.1:p.Leu826=
ENST00000545497.5:c.1956A>G	ENSP00000444640.2:p.Leu652=
ENST00000700553.1:c.2148A>G	ENSP00000515060.1:p.Leu716=
ENST00000700554.1:c.15A>G	ENSP00000515061.1:p.Leu5=
XM_011517921.1:c.2562A>G	XP_011516223.1:p.Leu854=
XM_011517922.1:c.2520A>G	XP_011516224.1:p.Leu840=
XM_011517923.1:c.2520A>G	XP_011516225.1:p.Leu840=
XM_011517924.1:c.2352A>G	XP_011516226.1:p.Leu784=
XM_011517924.2:c.2352A>G	XP_011516226.1:p.Leu784=
XM_011517925.1:c.2181A>G	XP_011516227.1:p.Leu727=
XM_011517926.1:c.2151A>G	XP_011516228.1:p.Leu717=
XM_011517927.1:c.1956A>G	XP_011516229.1:p.Leu652=
XM_011517928.1:c.2604A>G	XP_011516230.1:p.Leu868=
XM_011517929.1:c.1773A>G	XP_011516231.1:p.Leu591=
XM_011517930.1:c.1773A>G	XP_011516232.1:p.Leu591=
XM_011517931.1:c.1773A>G	XP_011516233.1:p.Leu591=
XM_011517932.1:c.1773A>G	XP_011516234.1:p.Leu591=
XM_011517933.1:c.2352A>G	XP_011516235.1:p.Leu784=
XM_011517934.1:c.1956A>G	XP_011516236.1:p.Leu652=
XM_011517934.2:c.1956A>G	XP_011516236.1:p.Leu652=
XM_017014816.1:c.2604A>G	XP_016870305.1:p.Leu868=
XM_017014817.1:c.2604A>G	XP_016870306.1:p.Leu868=
XM_017014818.1:c.2520A>G	XP_016870307.1:p.Leu840=
XM_017014819.1:c.2604A>G	XP_016870308.1:p.Leu868=
XM_017014820.1:c.2604A>G	XP_016870309.1:p.Leu868=
XM_017014821.1:c.2520A>G	XP_016870310.1:p.Leu840=
XM_017014822.1:c.2151A>G	XP_016870311.1:p.Leu717=
XM_017014823.1:c.2151A>G	XP_016870312.1:p.Leu717=
XM_017014824.1:c.1956A>G	XP_016870313.1:p.Leu652=
XM_017014825.2:c.2604A>G	XP_016870314.1:p.Leu868=
XM_017014826.1:c.2604A>G	XP_016870315.1:p.Leu868=
XM_017014827.1:c.2604A>G	XP_016870316.1:p.Leu868=
XM_017014828.1:c.2604A>G	XP_016870317.1:p.Leu868=
XM_017014829.2:c.1773A>G	XP_016870318.1:p.Leu591=