Canonical Allele Identifier: CA784487516

Gene: BANK1

Linked Data

• dbSNP Id: rs1271353092
• gnomAD v3: 4-101829798-C-CT
• gnomAD v4: 4-101829798-C-CT
• MyVariant Identifiers: chr4:g.102750955_102750956insT (hg19) ; chr4:g.101829798_101829799insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829803dup , CM000666.2:g.101829803dup	GRCh38
NC_000004.11:g.102750960dup , CM000666.1:g.102750960dup	GRCh37
NC_000004.10:g.102969983dup	NCBI36
NG_015824.1:g.44197dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-5dup MANE Select	ENSP00000320509.4:n.71-5dup
ENST00000322953.8:c.71-5dup	ENSP00000320509.4:n.71-5dup
ENST00000428908.5:c.71-25232dup	ENSP00000412748.1:n.71-25232dup
ENST00000444316.2:c.-20-5dup	ENSP00000388817.2:n.-20-5dup
ENST00000504592.5:c.26-5dup	ENSP00000421443.1:n.26-5dup
ENST00000508653.5:c.71-25232dup	ENSP00000422314.1:n.71-25232dup
NM_001083907.2:c.-20-5dup	NP_001077376.2:n.-20-5dup
NM_001127507.2:c.71-25232dup	NP_001120979.2:n.71-25232dup
NM_017935.4:c.71-5dup	NP_060405.4:n.71-5dup
XM_017008337.2:c.-20-5dup	XP_016863826.1:n.-20-5dup
NM_017935.5:c.71-5dup MANE Select	NP_060405.5:n.71-5dup
NM_001083907.3:c.-20-5dup	NP_001077376.3:n.-20-5dup
NM_001127507.3:c.71-25232dup	NP_001120979.3:n.71-25232dup