Canonical Allele Identifier: CA1481094971

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829761_101829762delinsCT , CM000666.2:g.101829761_101829762delinsCT	GRCh38
NC_000004.11:g.102750918_102750919delinsCT , CM000666.1:g.102750918_102750919delinsCT	GRCh37
NC_000004.10:g.102969941_102969942delinsCT	NCBI36
NG_015824.1:g.44155_44156delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-47_71-46delinsCT MANE Select	ENSP00000320509.4:n.71-47_71-46delinsCT
ENST00000322953.8:c.71-47_71-46delinsCT	ENSP00000320509.4:n.71-47_71-46delinsCT
ENST00000428908.5:c.71-25274_71-25273delinsCT	ENSP00000412748.1:n.71-25274_71-25273delinsCT
ENST00000444316.2:c.-20-47_-20-46delinsCT	ENSP00000388817.2:n.-20-47_-20-46delinsCT
ENST00000504592.5:c.26-47_26-46delinsCT	ENSP00000421443.1:n.26-47_26-46delinsCT
ENST00000508653.5:c.71-25274_71-25273delinsCT	ENSP00000422314.1:n.71-25274_71-25273delinsCT
NM_001083907.2:c.-20-47_-20-46delinsCT	NP_001077376.2:n.-20-47_-20-46delinsCT
NM_001127507.2:c.71-25274_71-25273delinsCT	NP_001120979.2:n.71-25274_71-25273delinsCT
NM_017935.4:c.71-47_71-46delinsCT	NP_060405.4:n.71-47_71-46delinsCT
XM_017008337.2:c.-20-47_-20-46delinsCT	XP_016863826.1:n.-20-47_-20-46delinsCT
NM_017935.5:c.71-47_71-46delinsCT MANE Select	NP_060405.5:n.71-47_71-46delinsCT
NM_001083907.3:c.-20-47_-20-46delinsCT	NP_001077376.3:n.-20-47_-20-46delinsCT
NM_001127507.3:c.71-25274_71-25273delinsCT	NP_001120979.3:n.71-25274_71-25273delinsCT