Canonical Allele Identifier: CA2762859688

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829480_101829481insGA , CM000666.2:g.101829480_101829481insGA	GRCh38
NC_000004.11:g.102750637_102750638insGA , CM000666.1:g.102750637_102750638insGA	GRCh37
NC_000004.10:g.102969660_102969661insGA	NCBI36
NG_015824.1:g.43874_43875insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-328_71-327insGA MANE Select	ENSP00000320509.4:n.71-328_71-327insGA
ENST00000322953.8:c.71-328_71-327insGA	ENSP00000320509.4:n.71-328_71-327insGA
ENST00000428908.5:c.71-25555_71-25554insGA	ENSP00000412748.1:n.71-25555_71-25554insGA
ENST00000444316.2:c.-20-328_-20-327insGA	ENSP00000388817.2:n.-20-328_-20-327insGA
ENST00000504592.5:c.26-328_26-327insGA	ENSP00000421443.1:n.26-328_26-327insGA
ENST00000508653.5:c.71-25555_71-25554insGA	ENSP00000422314.1:n.71-25555_71-25554insGA
NM_001083907.2:c.-20-328_-20-327insGA	NP_001077376.2:n.-20-328_-20-327insGA
NM_001127507.2:c.71-25555_71-25554insGA	NP_001120979.2:n.71-25555_71-25554insGA
NM_017935.4:c.71-328_71-327insGA	NP_060405.4:n.71-328_71-327insGA
XM_017008337.2:c.-20-328_-20-327insGA	XP_016863826.1:n.-20-328_-20-327insGA
NM_017935.5:c.71-328_71-327insGA MANE Select	NP_060405.5:n.71-328_71-327insGA
NM_001083907.3:c.-20-328_-20-327insGA	NP_001077376.3:n.-20-328_-20-327insGA
NM_001127507.3:c.71-25555_71-25554insGA	NP_001120979.3:n.71-25555_71-25554insGA