Canonical Allele Identifier: CA1481090071

Gene: BANK1

Linked Data

• dbSNP Id: rs1726014987

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818685_101818687del , CM000666.2:g.101818685_101818687del	GRCh38
NC_000004.11:g.102739842_102739844del , CM000666.1:g.102739842_102739844del	GRCh37
NC_000004.10:g.102958865_102958867del	NCBI36
NG_015824.1:g.33079_33081del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11123_71-11121del MANE Select	ENSP00000320509.4:n.71-11123_71-11121del
ENST00000322953.8:c.71-11123_71-11121del	ENSP00000320509.4:n.71-11123_71-11121del
ENST00000428908.5:c.70+27735_70+27737del	ENSP00000412748.1:n.70+27735_70+27737del
ENST00000444316.2:c.-21+4747_-21+4749del	ENSP00000388817.2:n.-21+4747_-21+4749del
ENST00000504592.5:c.26-11123_26-11121del	ENSP00000421443.1:n.26-11123_26-11121del
ENST00000508653.5:c.70+27735_70+27737del	ENSP00000422314.1:n.70+27735_70+27737del
NM_001083907.2:c.-21+4747_-21+4749del	NP_001077376.2:n.-21+4747_-21+4749del
NM_001127507.2:c.70+27735_70+27737del	NP_001120979.2:n.70+27735_70+27737del
NM_017935.4:c.71-11123_71-11121del	NP_060405.4:n.71-11123_71-11121del
XM_017008337.2:c.-20-11123_-20-11121del	XP_016863826.1:n.-20-11123_-20-11121del
NM_017935.5:c.71-11123_71-11121del MANE Select	NP_060405.5:n.71-11123_71-11121del
NM_001083907.3:c.-21+4747_-21+4749del	NP_001077376.3:n.-21+4747_-21+4749del
NM_001127507.3:c.70+27735_70+27737del	NP_001120979.3:n.70+27735_70+27737del