Canonical Allele Identifier: CA1066078755

Gene: BANK1

Linked Data

• dbSNP Id: rs1726518732
• gnomAD v3: 4-101829497-TTATC-T
• gnomAD v4: 4-101829497-TTATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829501_101829504del , CM000666.2:g.101829501_101829504del	GRCh38
NC_000004.11:g.102750658_102750661del , CM000666.1:g.102750658_102750661del	GRCh37
NC_000004.10:g.102969681_102969684del	NCBI36
NG_015824.1:g.43895_43898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-307_71-304del MANE Select	ENSP00000320509.4:n.71-307_71-304del
ENST00000322953.8:c.71-307_71-304del	ENSP00000320509.4:n.71-307_71-304del
ENST00000428908.5:c.71-25534_71-25531del	ENSP00000412748.1:n.71-25534_71-25531del
ENST00000444316.2:c.-20-307_-20-304del	ENSP00000388817.2:n.-20-307_-20-304del
ENST00000504592.5:c.26-307_26-304del	ENSP00000421443.1:n.26-307_26-304del
ENST00000508653.5:c.71-25534_71-25531del	ENSP00000422314.1:n.71-25534_71-25531del
NM_001083907.2:c.-20-307_-20-304del	NP_001077376.2:n.-20-307_-20-304del
NM_001127507.2:c.71-25534_71-25531del	NP_001120979.2:n.71-25534_71-25531del
NM_017935.4:c.71-307_71-304del	NP_060405.4:n.71-307_71-304del
XM_017008337.2:c.-20-307_-20-304del	XP_016863826.1:n.-20-307_-20-304del
NM_017935.5:c.71-307_71-304del MANE Select	NP_060405.5:n.71-307_71-304del
NM_001083907.3:c.-20-307_-20-304del	NP_001077376.3:n.-20-307_-20-304del
NM_001127507.3:c.71-25534_71-25531del	NP_001120979.3:n.71-25534_71-25531del