Canonical Allele Identifier: CA2578154626
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101917901del , CM000666.2:g.101917901del GRCh38
NC_000004.11:g.102839058del , CM000666.1:g.102839058del GRCh37
NC_000004.10:g.103058081del NCBI36
NG_015824.1:g.132295del

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.1010-92del MANE Select ENSP00000320509.4:n.1010-92del
ENST00000322953.8:c.1010-92del ENSP00000320509.4:n.1010-92del
ENST00000428908.5:c.611-92del ENSP00000412748.1:n.611-92del
ENST00000444316.2:c.920-92del ENSP00000388817.2:n.920-92del
ENST00000504592.5:c.965-92del ENSP00000421443.1:n.965-92del
ENST00000508653.5:c.611-92del ENSP00000422314.1:n.611-92del
NM_001083907.2:c.920-92del NP_001077376.2:n.920-92del
NM_001127507.2:c.611-92del NP_001120979.2:n.611-92del
NM_017935.4:c.1010-92del NP_060405.4:n.1010-92del
XM_017008337.2:c.920-92del XP_016863826.1:n.920-92del
NM_017935.5:c.1010-92del MANE Select NP_060405.5:n.1010-92del
NM_001083907.3:c.920-92del NP_001077376.3:n.920-92del
NM_001127507.3:c.611-92del NP_001120979.3:n.611-92del