Canonical Allele Identifier: CA784487368

Gene: BANK1

Linked Data

• dbSNP Id: rs1434447173
• MyVariant Identifiers: chr4:g.102750641_102750652del (hg19) ; chr4:g.101829484_101829495del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829493_101829504del , CM000666.2:g.101829493_101829504del	GRCh38
NC_000004.11:g.102750650_102750661del , CM000666.1:g.102750650_102750661del	GRCh37
NC_000004.10:g.102969673_102969684del	NCBI36
NG_015824.1:g.43887_43898del

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-315_71-304del MANE Select	ENSP00000320509.4:n.71-315_71-304del
ENST00000322953.8:c.71-315_71-304del	ENSP00000320509.4:n.71-315_71-304del
ENST00000428908.5:c.71-25542_71-25531del	ENSP00000412748.1:n.71-25542_71-25531del
ENST00000444316.2:c.-20-315_-20-304del	ENSP00000388817.2:n.-20-315_-20-304del
ENST00000504592.5:c.26-315_26-304del	ENSP00000421443.1:n.26-315_26-304del
ENST00000508653.5:c.71-25542_71-25531del	ENSP00000422314.1:n.71-25542_71-25531del
NM_001083907.2:c.-20-315_-20-304del	NP_001077376.2:n.-20-315_-20-304del
NM_001127507.2:c.71-25542_71-25531del	NP_001120979.2:n.71-25542_71-25531del
NM_017935.4:c.71-315_71-304del	NP_060405.4:n.71-315_71-304del
XM_017008337.2:c.-20-315_-20-304del	XP_016863826.1:n.-20-315_-20-304del
NM_017935.5:c.71-315_71-304del MANE Select	NP_060405.5:n.71-315_71-304del
NM_001083907.3:c.-20-315_-20-304del	NP_001077376.3:n.-20-315_-20-304del
NM_001127507.3:c.71-25542_71-25531del	NP_001120979.3:n.71-25542_71-25531del