Canonical Allele Identifier: CA204344
Community Standard Title: NM_017637.6(BNC2):c.84A>T (p.Ala28=)
Gene: BNC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.16738405T>A , CM000671.2:g.16738405T>A GRCh38
NC_000009.11:g.16738403T>A , CM000671.1:g.16738403T>A GRCh37
NC_000009.10:g.16728403T>A NCBI36
NG_051226.1:g.137434A>T

Transcript Alleles

HGVS Amino-acid Change
NM_017637.6:c.84A>T MANE Select NP_060107.3:p.Ala28=
ENST00000380672.9:c.84A>T MANE Select ENSP00000370047.3:p.Ala28=
NM_001317939.1:c.4-10408A>T NP_001304868.1:n.4-10408A>T
NM_001317939.2:c.4-10408A>T NP_001304868.1:n.4-10408A>T
NM_001317940.1:c.45+93839A>T NP_001304869.1:n.45+93839A>T
NM_001317940.2:c.45+93839A>T NP_001304869.1:n.45+93839A>T
NM_017637.5:c.84A>T NP_060107.3:p.Ala28=
ENST00000380666.6:c.-105-10408A>T ENSP00000370041.3:n.-105-10408A>T
ENST00000380667.6:c.84A>T ENSP00000370042.1:p.Ala28=
ENST00000380672.8:c.84A>T ENSP00000370047.3:p.Ala28=
ENST00000484726.5:c.84A>T ENSP00000431516.1:p.Ala28=
ENST00000486514.5:c.4-10408A>T ENSP00000474647.1:n.4-10408A>T
ENST00000545497.5:c.-393-10408A>T ENSP00000444640.2:n.-393-10408A>T
ENST00000613349.4:c.-105-10408A>T ENSP00000477717.1:n.-105-10408A>T
ENST00000617779.1:c.-151A>T ENSP00000482793.1:n.-151A>T
XM_011517921.1:c.84A>T XP_011516223.1:p.Ala28=
XM_011517922.1:c.126A>T XP_011516224.1:p.Ala42=
XM_011517923.1:c.126A>T XP_011516225.1:p.Ala42=
XM_011517924.1:c.4-10408A>T XP_011516226.1:n.4-10408A>T
XM_011517924.2:c.4-10408A>T XP_011516226.1:n.4-10408A>T
XM_011517926.1:c.3+132241A>T XP_011516228.1:n.3+132241A>T
XM_011517928.1:c.126A>T XP_011516230.1:p.Ala42=
XM_011517933.1:c.4-10408A>T XP_011516235.1:n.4-10408A>T
XM_017014816.1:c.126A>T XP_016870305.1:p.Ala42=
XM_017014817.1:c.126A>T XP_016870306.1:p.Ala42=
XM_017014818.1:c.126A>T XP_016870307.1:p.Ala42=
XM_017014819.1:c.126A>T XP_016870308.1:p.Ala42=
XM_017014820.1:c.126A>T XP_016870309.1:p.Ala42=
XM_017014821.1:c.126A>T XP_016870310.1:p.Ala42=
XM_017014825.2:c.126A>T XP_016870314.1:p.Ala42=
XM_017014826.1:c.126A>T XP_016870315.1:p.Ala42=
XM_017014827.1:c.126A>T XP_016870316.1:p.Ala42=
XM_017014828.1:c.126A>T XP_016870317.1:p.Ala42=