Canonical Allele Identifier: CA553732480

Gene: BANK1

Linked Data

• dbSNP Id: rs1475050385
• gnomAD v2: 4-102838919-CAAGT-C
• gnomAD v3: 4-101917762-CAAGT-C
• gnomAD v4: 4-101917762-CAAGT-C
• MyVariant Identifiers: chr4:g.102838920_102838923del (hg19) ; chr4:g.101917763_101917766del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101917766_101917769del , CM000666.2:g.101917766_101917769del	GRCh38
NC_000004.11:g.102838923_102838926del , CM000666.1:g.102838923_102838926del	GRCh37
NC_000004.10:g.103057946_103057949del	NCBI36
NG_015824.1:g.132160_132163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1010-227_1010-224del MANE Select	ENSP00000320509.4:n.1010-227_1010-224del
ENST00000322953.8:c.1010-227_1010-224del	ENSP00000320509.4:n.1010-227_1010-224del
ENST00000428908.5:c.611-227_611-224del	ENSP00000412748.1:n.611-227_611-224del
ENST00000444316.2:c.920-227_920-224del	ENSP00000388817.2:n.920-227_920-224del
ENST00000504592.5:c.965-227_965-224del	ENSP00000421443.1:n.965-227_965-224del
ENST00000508653.5:c.611-227_611-224del	ENSP00000422314.1:n.611-227_611-224del
NM_001083907.2:c.920-227_920-224del	NP_001077376.2:n.920-227_920-224del
NM_001127507.2:c.611-227_611-224del	NP_001120979.2:n.611-227_611-224del
NM_017935.4:c.1010-227_1010-224del	NP_060405.4:n.1010-227_1010-224del
XM_017008337.2:c.920-227_920-224del	XP_016863826.1:n.920-227_920-224del
NM_017935.5:c.1010-227_1010-224del MANE Select	NP_060405.5:n.1010-227_1010-224del
NM_001083907.3:c.920-227_920-224del	NP_001077376.3:n.920-227_920-224del
NM_001127507.3:c.611-227_611-224del	NP_001120979.3:n.611-227_611-224del