Canonical Allele Identifier: CA784480539

Gene: BANK1

Linked Data

• dbSNP Id: rs1479387263
• MyVariant Identifiers: chr4:g.102739785_102739786insAG (hg19) ; chr4:g.101818628_101818629insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818632_101818633dup , CM000666.2:g.101818632_101818633dup	GRCh38
NC_000004.11:g.102739789_102739790dup , CM000666.1:g.102739789_102739790dup	GRCh37
NC_000004.10:g.102958812_102958813dup	NCBI36
NG_015824.1:g.33026_33027dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11176_71-11175dup MANE Select	ENSP00000320509.4:n.71-11176_71-11175dup
ENST00000322953.8:c.71-11176_71-11175dup	ENSP00000320509.4:n.71-11176_71-11175dup
ENST00000428908.5:c.70+27682_70+27683dup	ENSP00000412748.1:n.70+27682_70+27683dup
ENST00000444316.2:c.-21+4694_-21+4695dup	ENSP00000388817.2:n.-21+4694_-21+4695dup
ENST00000504592.5:c.26-11176_26-11175dup	ENSP00000421443.1:n.26-11176_26-11175dup
ENST00000508653.5:c.70+27682_70+27683dup	ENSP00000422314.1:n.70+27682_70+27683dup
NM_001083907.2:c.-21+4694_-21+4695dup	NP_001077376.2:n.-21+4694_-21+4695dup
NM_001127507.2:c.70+27682_70+27683dup	NP_001120979.2:n.70+27682_70+27683dup
NM_017935.4:c.71-11176_71-11175dup	NP_060405.4:n.71-11176_71-11175dup
XM_017008337.2:c.-20-11176_-20-11175dup	XP_016863826.1:n.-20-11176_-20-11175dup
NM_017935.5:c.71-11176_71-11175dup MANE Select	NP_060405.5:n.71-11176_71-11175dup
NM_001083907.3:c.-21+4694_-21+4695dup	NP_001077376.3:n.-21+4694_-21+4695dup
NM_001127507.3:c.70+27682_70+27683dup	NP_001120979.3:n.70+27682_70+27683dup