Canonical Allele Identifier: CA1066075646

Gene: BANK1

Linked Data

• dbSNP Id: rs1726013490
• gnomAD v3: 4-101818633-A-AG
• gnomAD v4: 4-101818633-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818633_101818634insG , CM000666.2:g.101818633_101818634insG	GRCh38
NC_000004.11:g.102739790_102739791insG , CM000666.1:g.102739790_102739791insG	GRCh37
NC_000004.10:g.102958813_102958814insG	NCBI36
NG_015824.1:g.33027_33028insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11175_71-11174insG MANE Select	ENSP00000320509.4:n.71-11175_71-11174insG
ENST00000322953.8:c.71-11175_71-11174insG	ENSP00000320509.4:n.71-11175_71-11174insG
ENST00000428908.5:c.70+27683_70+27684insG	ENSP00000412748.1:n.70+27683_70+27684insG
ENST00000444316.2:c.-21+4695_-21+4696insG	ENSP00000388817.2:n.-21+4695_-21+4696insG
ENST00000504592.5:c.26-11175_26-11174insG	ENSP00000421443.1:n.26-11175_26-11174insG
ENST00000508653.5:c.70+27683_70+27684insG	ENSP00000422314.1:n.70+27683_70+27684insG
NM_001083907.2:c.-21+4695_-21+4696insG	NP_001077376.2:n.-21+4695_-21+4696insG
NM_001127507.2:c.70+27683_70+27684insG	NP_001120979.2:n.70+27683_70+27684insG
NM_017935.4:c.71-11175_71-11174insG	NP_060405.4:n.71-11175_71-11174insG
XM_017008337.2:c.-20-11175_-20-11174insG	XP_016863826.1:n.-20-11175_-20-11174insG
NM_017935.5:c.71-11175_71-11174insG MANE Select	NP_060405.5:n.71-11175_71-11174insG
NM_001083907.3:c.-21+4695_-21+4696insG	NP_001077376.3:n.-21+4695_-21+4696insG
NM_001127507.3:c.70+27683_70+27684insG	NP_001120979.3:n.70+27683_70+27684insG