Canonical Allele Identifier: CA2671564686
Gene: BANK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101918145del , CM000666.2:g.101918145del GRCh38
NC_000004.11:g.102839302del , CM000666.1:g.102839302del GRCh37
NC_000004.10:g.103058325del NCBI36
NG_015824.1:g.132539del

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.1162del MANE Select ENSP00000320509.4:p.Arg388GlyfsTer21
ENST00000322953.8:c.1162del ENSP00000320509.4:p.Arg388GlyfsTer21
ENST00000428908.5:c.763del ENSP00000412748.1:p.Arg255GlyfsTer21
ENST00000444316.2:c.1072del ENSP00000388817.2:p.Arg358GlyfsTer21
ENST00000504592.5:c.1117del ENSP00000421443.1:p.Arg373GlyfsTer21
ENST00000508653.5:c.763del ENSP00000422314.1:p.Arg255GlyfsTer21
NM_001083907.2:c.1072del NP_001077376.2:p.Arg358GlyfsTer21
NM_001127507.2:c.763del NP_001120979.2:p.Arg255GlyfsTer21
NM_017935.4:c.1162del NP_060405.4:p.Arg388GlyfsTer21
XM_017008337.2:c.1072del XP_016863826.1:p.Arg358GlyfsTer21
NM_017935.5:c.1162del MANE Select NP_060405.5:p.Arg388GlyfsTer21
NM_001083907.3:c.1072del NP_001077376.3:p.Arg358GlyfsTer21
NM_001127507.3:c.763del NP_001120979.3:p.Arg255GlyfsTer21