Canonical Allele Identifier: CA784487467

Gene: BANK1

Linked Data

• dbSNP Id: rs1245663939
• gnomAD v4: 4-101829656-A-AT
• MyVariant Identifiers: chr4:g.102750813_102750814insT (hg19) ; chr4:g.101829656_101829657insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829662dup , CM000666.2:g.101829662dup	GRCh38
NC_000004.11:g.102750819dup , CM000666.1:g.102750819dup	GRCh37
NC_000004.10:g.102969842dup	NCBI36
NG_015824.1:g.44056dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-146dup MANE Select	ENSP00000320509.4:n.71-146dup
ENST00000322953.8:c.71-146dup	ENSP00000320509.4:n.71-146dup
ENST00000428908.5:c.71-25373dup	ENSP00000412748.1:n.71-25373dup
ENST00000444316.2:c.-20-146dup	ENSP00000388817.2:n.-20-146dup
ENST00000504592.5:c.26-146dup	ENSP00000421443.1:n.26-146dup
ENST00000508653.5:c.71-25373dup	ENSP00000422314.1:n.71-25373dup
NM_001083907.2:c.-20-146dup	NP_001077376.2:n.-20-146dup
NM_001127507.2:c.71-25373dup	NP_001120979.2:n.71-25373dup
NM_017935.4:c.71-146dup	NP_060405.4:n.71-146dup
XM_017008337.2:c.-20-146dup	XP_016863826.1:n.-20-146dup
NM_017935.5:c.71-146dup MANE Select	NP_060405.5:n.71-146dup
NM_001083907.3:c.-20-146dup	NP_001077376.3:n.-20-146dup
NM_001127507.3:c.71-25373dup	NP_001120979.3:n.71-25373dup