Canonical Allele Identifier: CA1481131991

Gene: BANK1

Linked Data

• dbSNP Id: rs1389708990

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101943954dup , CM000666.2:g.101943954dup	GRCh38
NC_000004.11:g.102865111dup , CM000666.1:g.102865111dup	GRCh37
NC_000004.10:g.103084134dup	NCBI36
NG_015824.1:g.158348dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+25765dup MANE Select	ENSP00000320509.4:n.1206+25765dup
ENST00000322953.8:c.1206+25765dup	ENSP00000320509.4:n.1206+25765dup
ENST00000428908.5:c.807+25765dup	ENSP00000412748.1:n.807+25765dup
ENST00000444316.2:c.1116+25765dup	ENSP00000388817.2:n.1116+25765dup
ENST00000504592.5:c.1161+25765dup	ENSP00000421443.1:n.1161+25765dup
ENST00000508653.5:c.807+25765dup	ENSP00000422314.1:n.807+25765dup
NM_001083907.2:c.1116+25765dup	NP_001077376.2:n.1116+25765dup
NM_001127507.2:c.807+25765dup	NP_001120979.2:n.807+25765dup
NM_017935.4:c.1206+25765dup	NP_060405.4:n.1206+25765dup
XM_017008337.2:c.1116+25765dup	XP_016863826.1:n.1116+25765dup
NM_017935.5:c.1206+25765dup MANE Select	NP_060405.5:n.1206+25765dup
NM_001083907.3:c.1116+25765dup	NP_001077376.3:n.1116+25765dup
NM_001127507.3:c.807+25765dup	NP_001120979.3:n.807+25765dup