Canonical Allele Identifier: CA1481132072

Gene: BANK1

Linked Data

• dbSNP Id: rs1282908802

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944022_101944027dup , CM000666.2:g.101944022_101944027dup	GRCh38
NC_000004.11:g.102865179_102865184dup , CM000666.1:g.102865179_102865184dup	GRCh37
NC_000004.10:g.103084202_103084207dup	NCBI36
NG_015824.1:g.158416_158421dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+25833_1206+25838dup MANE Select	ENSP00000320509.4:n.1206+25833_1206+25838dup
ENST00000322953.8:c.1206+25833_1206+25838dup	ENSP00000320509.4:n.1206+25833_1206+25838dup
ENST00000428908.5:c.807+25833_807+25838dup	ENSP00000412748.1:n.807+25833_807+25838dup
ENST00000444316.2:c.1116+25833_1116+25838dup	ENSP00000388817.2:n.1116+25833_1116+25838dup
ENST00000504592.5:c.1161+25833_1161+25838dup	ENSP00000421443.1:n.1161+25833_1161+25838dup
ENST00000508653.5:c.807+25833_807+25838dup	ENSP00000422314.1:n.807+25833_807+25838dup
NM_001083907.2:c.1116+25833_1116+25838dup	NP_001077376.2:n.1116+25833_1116+25838dup
NM_001127507.2:c.807+25833_807+25838dup	NP_001120979.2:n.807+25833_807+25838dup
NM_017935.4:c.1206+25833_1206+25838dup	NP_060405.4:n.1206+25833_1206+25838dup
XM_017008337.2:c.1116+25833_1116+25838dup	XP_016863826.1:n.1116+25833_1116+25838dup
NM_017935.5:c.1206+25833_1206+25838dup MANE Select	NP_060405.5:n.1206+25833_1206+25838dup
NM_001083907.3:c.1116+25833_1116+25838dup	NP_001077376.3:n.1116+25833_1116+25838dup
NM_001127507.3:c.807+25833_807+25838dup	NP_001120979.3:n.807+25833_807+25838dup