Canonical Allele Identifier: CA2671564688

Gene: BANK1

Linked Data

• gnomAD v4: 4-101918183-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918187del , CM000666.2:g.101918187del	GRCh38
NC_000004.11:g.102839344del , CM000666.1:g.102839344del	GRCh37
NC_000004.10:g.103058367del	NCBI36
NG_015824.1:g.132581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1204del MANE Select	ENSP00000320509.4:p.Ser402GlnfsTer7
ENST00000322953.8:c.1204del	ENSP00000320509.4:p.Ser402GlnfsTer7
ENST00000428908.5:c.805del	ENSP00000412748.1:p.Ser269GlnfsTer7
ENST00000444316.2:c.1114del	ENSP00000388817.2:p.Ser372GlnfsTer7
ENST00000504592.5:c.1159del	ENSP00000421443.1:p.Ser387GlnfsTer7
ENST00000508653.5:c.805del	ENSP00000422314.1:p.Ser269GlnfsTer7
NM_001083907.2:c.1114del	NP_001077376.2:p.Ser372GlnfsTer7
NM_001127507.2:c.805del	NP_001120979.2:p.Ser269GlnfsTer7
NM_017935.4:c.1204del	NP_060405.4:p.Ser402GlnfsTer7
XM_017008337.2:c.1114del	XP_016863826.1:p.Ser372GlnfsTer7
NM_017935.5:c.1204del MANE Select	NP_060405.5:p.Ser402GlnfsTer7
NM_001083907.3:c.1114del	NP_001077376.3:p.Ser372GlnfsTer7
NM_001127507.3:c.805del	NP_001120979.3:p.Ser269GlnfsTer7