Canonical Allele Identifier: CA1481088867

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101815970_101815974delinsCCTAA , CM000666.2:g.101815970_101815974delinsCCTAA	GRCh38
NC_000004.11:g.102737127_102737131delinsCCTAA , CM000666.1:g.102737127_102737131delinsCCTAA	GRCh37
NC_000004.10:g.102956150_102956154delinsCCTAA	NCBI36
NG_015824.1:g.30364_30368delinsCCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-13838_71-13834delinsCCTAA MANE Select	ENSP00000320509.4:n.71-13838_71-13834delinsCCTAA
ENST00000322953.8:c.71-13838_71-13834delinsCCTAA	ENSP00000320509.4:n.71-13838_71-13834delinsCCTAA
ENST00000428908.5:c.70+25020_70+25024delinsCCTAA	ENSP00000412748.1:n.70+25020_70+25024delinsCCTAA
ENST00000444316.2:c.-21+2032_-21+2036delinsCCTAA	ENSP00000388817.2:n.-21+2032_-21+2036delinsCCTAA
ENST00000504592.5:c.26-13838_26-13834delinsCCTAA	ENSP00000421443.1:n.26-13838_26-13834delinsCCTAA
ENST00000508653.5:c.70+25020_70+25024delinsCCTAA	ENSP00000422314.1:n.70+25020_70+25024delinsCCTAA
NM_001083907.2:c.-21+2032_-21+2036delinsCCTAA	NP_001077376.2:n.-21+2032_-21+2036delinsCCTAA
NM_001127507.2:c.70+25020_70+25024delinsCCTAA	NP_001120979.2:n.70+25020_70+25024delinsCCTAA
NM_017935.4:c.71-13838_71-13834delinsCCTAA	NP_060405.4:n.71-13838_71-13834delinsCCTAA
XM_017008337.2:c.-20-13838_-20-13834delinsCCTAA	XP_016863826.1:n.-20-13838_-20-13834delinsCCTAA
NM_017935.5:c.71-13838_71-13834delinsCCTAA MANE Select	NP_060405.5:n.71-13838_71-13834delinsCCTAA
NM_001083907.3:c.-21+2032_-21+2036delinsCCTAA	NP_001077376.3:n.-21+2032_-21+2036delinsCCTAA
NM_001127507.3:c.70+25020_70+25024delinsCCTAA	NP_001120979.3:n.70+25020_70+25024delinsCCTAA