Canonical Allele Identifier: CA4995637

Gene: BNC2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.16419272G>A , CM000671.2:g.16419272G>A	GRCh38
NC_000009.11:g.16419270G>A , CM000671.1:g.16419270G>A	GRCh37
NC_000009.10:g.16409270G>A	NCBI36
NG_051226.1:g.456567C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700553.1:c.2753C>T	ENSP00000515060.1:p.Ala918Val
ENST00000380672.9:c.3017C>T MANE Select	ENSP00000370047.3:p.Ala1006Val
ENST00000380667.6:c.2816C>T	ENSP00000370042.1:p.Ala939Val
ENST00000380672.8:c.3017C>T	ENSP00000370047.3:p.Ala1006Val
ENST00000411752.5:c.1377C>T	ENSP00000392212.1:n.1377C>T
ENST00000418777.5:c.2944C>T	ENSP00000408370.1:n.2944C>T
ENST00000484726.5:c.*1039C>T	ENSP00000431516.1:n.*1039C>T
ENST00000545497.5:c.*361C>T	ENSP00000444640.2:n.*361C>T
NM_017637.5:c.3017C>T	NP_060107.3:p.Ala1006Val
XM_011517921.1:c.3242C>T	XP_011516223.1:p.Ala1081Val
XM_011517922.1:c.3200C>T	XP_011516224.1:p.Ala1067Val
XM_011517923.1:c.3059C>T	XP_011516225.1:p.Ala1020Val
XM_011517924.1:c.3032C>T	XP_011516226.1:p.Ala1011Val
XM_011517925.1:c.2861C>T	XP_011516227.1:p.Ala954Val
XM_011517926.1:c.2831C>T	XP_011516228.1:p.Ala944Val
XM_011517927.1:c.2636C>T	XP_011516229.1:p.Ala879Val
XM_011517928.1:c.*361C>T	XP_011516230.1:n.*361C>T
XM_011517929.1:c.2453C>T	XP_011516231.1:p.Ala818Val
XM_011517930.1:c.2453C>T	XP_011516232.1:p.Ala818Val
XM_011517931.1:c.2453C>T	XP_011516233.1:p.Ala818Val
XM_011517932.1:c.2453C>T	XP_011516234.1:p.Ala818Val
XM_011517933.1:c.*361C>T	XP_011516235.1:n.*361C>T
NM_001317939.1:c.*361C>T	NP_001304868.1:n.*361C>T
NM_001317940.1:c.2732C>T	NP_001304869.1:p.Ala911Val
XM_011517924.2:c.3032C>T	XP_011516226.1:p.Ala1011Val
XM_017014816.1:c.3284C>T	XP_016870305.1:p.Ala1095Val
XM_017014817.1:c.3209C>T	XP_016870306.1:p.Ala1070Val
XM_017014818.1:c.3200C>T	XP_016870307.1:p.Ala1067Val
XM_017014819.1:c.3143C>T	XP_016870308.1:p.Ala1048Val
XM_017014820.1:c.3137C>T	XP_016870309.1:p.Ala1046Val
XM_017014821.1:c.3059C>T	XP_016870310.1:p.Ala1020Val
XM_017014822.1:c.2831C>T	XP_016870311.1:p.Ala944Val
XM_017014823.1:c.2831C>T	XP_016870312.1:p.Ala944Val
XM_017014824.1:c.2636C>T	XP_016870313.1:p.Ala879Val
XM_017014825.2:c.*393C>T	XP_016870314.1:n.*393C>T
XM_017014826.1:c.*361C>T	XP_016870315.1:n.*361C>T
XM_017014829.2:c.*393C>T	XP_016870318.1:n.*393C>T
NM_017637.6:c.3017C>T MANE Select	NP_060107.3:p.Ala1006Val
NM_001317939.2:c.*361C>T	NP_001304868.1:n.*361C>T
NM_001317940.2:c.2732C>T	NP_001304869.1:p.Ala911Val