Canonical Allele Identifier: CA553722761

Gene: BANK1

Linked Data

• dbSNP Id: rs1481577762
• gnomAD v2: 4-102865357-G-A
• gnomAD v3: 4-101944200-G-A
• gnomAD v4: 4-101944200-G-A
• MyVariant Identifiers: chr4:g.102865357G>A (hg19) ; chr4:g.101944200G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944200G>A , CM000666.2:g.101944200G>A	GRCh38
NC_000004.11:g.102865357G>A , CM000666.1:g.102865357G>A	GRCh37
NC_000004.10:g.103084380G>A	NCBI36
NG_015824.1:g.158594G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1206+26011G>A MANE Select	ENSP00000320509.4:n.1206+26011G>A
ENST00000322953.8:c.1206+26011G>A	ENSP00000320509.4:n.1206+26011G>A
ENST00000428908.5:c.807+26011G>A	ENSP00000412748.1:n.807+26011G>A
ENST00000444316.2:c.1116+26011G>A	ENSP00000388817.2:n.1116+26011G>A
ENST00000504592.5:c.1161+26011G>A	ENSP00000421443.1:n.1161+26011G>A
ENST00000508653.5:c.807+26011G>A	ENSP00000422314.1:n.807+26011G>A
NM_001083907.2:c.1116+26011G>A	NP_001077376.2:n.1116+26011G>A
NM_001127507.2:c.807+26011G>A	NP_001120979.2:n.807+26011G>A
NM_017935.4:c.1206+26011G>A	NP_060405.4:n.1206+26011G>A
XM_017008337.2:c.1116+26011G>A	XP_016863826.1:n.1116+26011G>A
NM_017935.5:c.1206+26011G>A MANE Select	NP_060405.5:n.1206+26011G>A
NM_001083907.3:c.1116+26011G>A	NP_001077376.3:n.1116+26011G>A
NM_001127507.3:c.807+26011G>A	NP_001120979.3:n.807+26011G>A