Canonical Allele Identifier: CA190569651

Gene: BNC2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.16727831G>C , CM000671.2:g.16727831G>C	GRCh38
NC_000009.11:g.16727829G>C , CM000671.1:g.16727829G>C	GRCh37
NC_000009.10:g.16717829G>C	NCBI36
NG_051226.1:g.148008C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_017637.6:c.296C>G MANE Select	NP_060107.3:p.Ala99Gly
ENST00000380672.9:c.296C>G MANE Select	ENSP00000370047.3:p.Ala99Gly
NM_001317939.1:c.170C>G	NP_001304868.1:p.Ala57Gly
NM_001317939.2:c.170C>G	NP_001304868.1:p.Ala57Gly
NM_001317940.1:c.45+104413C>G	NP_001304869.1:n.45+104413C>G
NM_001317940.2:c.45+104413C>G	NP_001304869.1:n.45+104413C>G
NM_017637.5:c.296C>G	NP_060107.3:p.Ala99Gly
ENST00000380666.6:c.62C>G	ENSP00000370041.3:p.Ala21Gly
ENST00000380667.6:c.129+10529C>G	ENSP00000370042.1:n.129+10529C>G
ENST00000380672.8:c.296C>G	ENSP00000370047.3:p.Ala99Gly
ENST00000418777.5:c.167C>G	ENSP00000408370.1:p.Ala56Gly
ENST00000468187.6:c.167C>G	ENSP00000474468.1:p.Ala56Gly
ENST00000484726.5:c.296C>G	ENSP00000431516.1:p.Ala99Gly
ENST00000486514.5:c.170C>G	ENSP00000474647.1:p.Ala57Gly
ENST00000545497.5:c.-227C>G	ENSP00000444640.2:n.-227C>G
ENST00000603313.5:c.62C>G	ENSP00000473935.1:p.Ala21Gly
ENST00000603713.5:c.62C>G	ENSP00000474045.1:p.Ala21Gly
ENST00000613349.4:c.62C>G	ENSP00000477717.1:p.Ala21Gly
ENST00000617779.1:c.62C>G	ENSP00000482793.1:p.Ala21Gly
XM_011517921.1:c.296C>G	XP_011516223.1:p.Ala99Gly
XM_011517922.1:c.338C>G	XP_011516224.1:p.Ala113Gly
XM_011517923.1:c.338C>G	XP_011516225.1:p.Ala113Gly
XM_011517924.1:c.170C>G	XP_011516226.1:p.Ala57Gly
XM_011517924.2:c.170C>G	XP_011516226.1:p.Ala57Gly
XM_011517926.1:c.3+142815C>G	XP_011516228.1:n.3+142815C>G
XM_011517928.1:c.338C>G	XP_011516230.1:p.Ala113Gly
XM_011517933.1:c.170C>G	XP_011516235.1:p.Ala57Gly
XM_017014816.1:c.338C>G	XP_016870305.1:p.Ala113Gly
XM_017014817.1:c.338C>G	XP_016870306.1:p.Ala113Gly
XM_017014818.1:c.338C>G	XP_016870307.1:p.Ala113Gly
XM_017014819.1:c.338C>G	XP_016870308.1:p.Ala113Gly
XM_017014820.1:c.338C>G	XP_016870309.1:p.Ala113Gly
XM_017014821.1:c.338C>G	XP_016870310.1:p.Ala113Gly
XM_017014825.2:c.338C>G	XP_016870314.1:p.Ala113Gly
XM_017014826.1:c.338C>G	XP_016870315.1:p.Ala113Gly
XM_017014827.1:c.338C>G	XP_016870316.1:p.Ala113Gly
XM_017014828.1:c.338C>G	XP_016870317.1:p.Ala113Gly