Canonical Allele Identifier: CA2512942449

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944070_101944075del , CM000666.2:g.101944070_101944075del	GRCh38
NC_000004.11:g.102865227_102865232del , CM000666.1:g.102865227_102865232del	GRCh37
NC_000004.10:g.103084250_103084255del	NCBI36
NG_015824.1:g.158464_158469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+25881_1206+25886del MANE Select	ENSP00000320509.4:n.1206+25881_1206+25886del
ENST00000322953.8:c.1206+25881_1206+25886del	ENSP00000320509.4:n.1206+25881_1206+25886del
ENST00000428908.5:c.807+25881_807+25886del	ENSP00000412748.1:n.807+25881_807+25886del
ENST00000444316.2:c.1116+25881_1116+25886del	ENSP00000388817.2:n.1116+25881_1116+25886del
ENST00000504592.5:c.1161+25881_1161+25886del	ENSP00000421443.1:n.1161+25881_1161+25886del
ENST00000508653.5:c.807+25881_807+25886del	ENSP00000422314.1:n.807+25881_807+25886del
NM_001083907.2:c.1116+25881_1116+25886del	NP_001077376.2:n.1116+25881_1116+25886del
NM_001127507.2:c.807+25881_807+25886del	NP_001120979.2:n.807+25881_807+25886del
NM_017935.4:c.1206+25881_1206+25886del	NP_060405.4:n.1206+25881_1206+25886del
XM_017008337.2:c.1116+25881_1116+25886del	XP_016863826.1:n.1116+25881_1116+25886del
NM_017935.5:c.1206+25881_1206+25886del MANE Select	NP_060405.5:n.1206+25881_1206+25886del
NM_001083907.3:c.1116+25881_1116+25886del	NP_001077376.3:n.1116+25881_1116+25886del
NM_001127507.3:c.807+25881_807+25886del	NP_001120979.3:n.807+25881_807+25886del