Canonical Allele Identifier: CA1066075931
Gene: BANK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101818901_101818905del , CM000666.2:g.101818901_101818905del GRCh38
NC_000004.11:g.102740058_102740062del , CM000666.1:g.102740058_102740062del GRCh37
NC_000004.10:g.102959081_102959085del NCBI36
NG_015824.1:g.33295_33299del

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.71-10907_71-10903del MANE Select ENSP00000320509.4:n.71-10907_71-10903del
ENST00000322953.8:c.71-10907_71-10903del ENSP00000320509.4:n.71-10907_71-10903del
ENST00000428908.5:c.70+27951_70+27955del ENSP00000412748.1:n.70+27951_70+27955del
ENST00000444316.2:c.-21+4963_-21+4967del ENSP00000388817.2:n.-21+4963_-21+4967del
ENST00000504592.5:c.26-10907_26-10903del ENSP00000421443.1:n.26-10907_26-10903del
ENST00000508653.5:c.70+27951_70+27955del ENSP00000422314.1:n.70+27951_70+27955del
NM_001083907.2:c.-21+4963_-21+4967del NP_001077376.2:n.-21+4963_-21+4967del
NM_001127507.2:c.70+27951_70+27955del NP_001120979.2:n.70+27951_70+27955del
NM_017935.4:c.71-10907_71-10903del NP_060405.4:n.71-10907_71-10903del
XM_017008337.2:c.-20-10907_-20-10903del XP_016863826.1:n.-20-10907_-20-10903del
NM_017935.5:c.71-10907_71-10903del MANE Select NP_060405.5:n.71-10907_71-10903del
NM_001083907.3:c.-21+4963_-21+4967del NP_001077376.3:n.-21+4963_-21+4967del
NM_001127507.3:c.70+27951_70+27955del NP_001120979.3:n.70+27951_70+27955del