Canonical Allele Identifier: CA2671540422
Gene: BANK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101829702del , CM000666.2:g.101829702del GRCh38
NC_000004.11:g.102750859del , CM000666.1:g.102750859del GRCh37
NC_000004.10:g.102969882del NCBI36
NG_015824.1:g.44096del

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.71-106del MANE Select ENSP00000320509.4:n.71-106del
ENST00000322953.8:c.71-106del ENSP00000320509.4:n.71-106del
ENST00000428908.5:c.71-25333del ENSP00000412748.1:n.71-25333del
ENST00000444316.2:c.-20-106del ENSP00000388817.2:n.-20-106del
ENST00000504592.5:c.26-106del ENSP00000421443.1:n.26-106del
ENST00000508653.5:c.71-25333del ENSP00000422314.1:n.71-25333del
NM_001083907.2:c.-20-106del NP_001077376.2:n.-20-106del
NM_001127507.2:c.71-25333del NP_001120979.2:n.71-25333del
NM_017935.4:c.71-106del NP_060405.4:n.71-106del
XM_017008337.2:c.-20-106del XP_016863826.1:n.-20-106del
NM_017935.5:c.71-106del MANE Select NP_060405.5:n.71-106del
NM_001083907.3:c.-20-106del NP_001077376.3:n.-20-106del
NM_001127507.3:c.71-25333del NP_001120979.3:n.71-25333del