Canonical Allele Identifier: CA1481094875
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101829536_101829539delinsTTTA , CM000666.2:g.101829536_101829539delinsTTTA GRCh38
NC_000004.11:g.102750693_102750696delinsTTTA , CM000666.1:g.102750693_102750696delinsTTTA GRCh37
NC_000004.10:g.102969716_102969719delinsTTTA NCBI36
NG_015824.1:g.43930_43933delinsTTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.71-272_71-269delinsTTTA MANE Select ENSP00000320509.4:n.71-272_71-269delinsTTTA
ENST00000322953.8:c.71-272_71-269delinsTTTA ENSP00000320509.4:n.71-272_71-269delinsTTTA
ENST00000428908.5:c.71-25499_71-25496delinsTTTA ENSP00000412748.1:n.71-25499_71-25496delinsTTTA
ENST00000444316.2:c.-20-272_-20-269delinsTTTA ENSP00000388817.2:n.-20-272_-20-269delinsTTTA
ENST00000504592.5:c.26-272_26-269delinsTTTA ENSP00000421443.1:n.26-272_26-269delinsTTTA
ENST00000508653.5:c.71-25499_71-25496delinsTTTA ENSP00000422314.1:n.71-25499_71-25496delinsTTTA
NM_001083907.2:c.-20-272_-20-269delinsTTTA NP_001077376.2:n.-20-272_-20-269delinsTTTA
NM_001127507.2:c.71-25499_71-25496delinsTTTA NP_001120979.2:n.71-25499_71-25496delinsTTTA
NM_017935.4:c.71-272_71-269delinsTTTA NP_060405.4:n.71-272_71-269delinsTTTA
XM_017008337.2:c.-20-272_-20-269delinsTTTA XP_016863826.1:n.-20-272_-20-269delinsTTTA
NM_017935.5:c.71-272_71-269delinsTTTA MANE Select NP_060405.5:n.71-272_71-269delinsTTTA
NM_001083907.3:c.-20-272_-20-269delinsTTTA NP_001077376.3:n.-20-272_-20-269delinsTTTA
NM_001127507.3:c.71-25499_71-25496delinsTTTA NP_001120979.3:n.71-25499_71-25496delinsTTTA