Canonical Allele Identifier: CA103059585

Gene: BANK1

Linked Data

• dbSNP Id: rs1024994142
• gnomAD v2: 4-102739759-C-CA
• gnomAD v3: 4-101818602-C-CA
• gnomAD v4: 4-101818602-C-CA
• MyVariant Identifiers: chr4:g.102739759_102739760insA (hg19) ; chr4:g.101818602_101818603insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818607dup , CM000666.2:g.101818607dup	GRCh38
NC_000004.11:g.102739764dup , CM000666.1:g.102739764dup	GRCh37
NC_000004.10:g.102958787dup	NCBI36
NG_015824.1:g.33001dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11201dup MANE Select	ENSP00000320509.4:n.71-11201dup
ENST00000322953.8:c.71-11201dup	ENSP00000320509.4:n.71-11201dup
ENST00000428908.5:c.70+27657dup	ENSP00000412748.1:n.70+27657dup
ENST00000444316.2:c.-21+4669dup	ENSP00000388817.2:n.-21+4669dup
ENST00000504592.5:c.26-11201dup	ENSP00000421443.1:n.26-11201dup
ENST00000508653.5:c.70+27657dup	ENSP00000422314.1:n.70+27657dup
NM_001083907.2:c.-21+4669dup	NP_001077376.2:n.-21+4669dup
NM_001127507.2:c.70+27657dup	NP_001120979.2:n.70+27657dup
NM_017935.4:c.71-11201dup	NP_060405.4:n.71-11201dup
XM_017008337.2:c.-20-11201dup	XP_016863826.1:n.-20-11201dup
NM_017935.5:c.71-11201dup MANE Select	NP_060405.5:n.71-11201dup
NM_001083907.3:c.-21+4669dup	NP_001077376.3:n.-21+4669dup
NM_001127507.3:c.70+27657dup	NP_001120979.3:n.70+27657dup