Canonical Allele Identifier: CA1066075943

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818907_101818910del , CM000666.2:g.101818907_101818910del	GRCh38
NC_000004.11:g.102740064_102740067del , CM000666.1:g.102740064_102740067del	GRCh37
NC_000004.10:g.102959087_102959090del	NCBI36
NG_015824.1:g.33301_33304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10901_71-10898del MANE Select	ENSP00000320509.4:n.71-10901_71-10898del
ENST00000322953.8:c.71-10901_71-10898del	ENSP00000320509.4:n.71-10901_71-10898del
ENST00000428908.5:c.70+27957_70+27960del	ENSP00000412748.1:n.70+27957_70+27960del
ENST00000444316.2:c.-21+4969_-21+4972del	ENSP00000388817.2:n.-21+4969_-21+4972del
ENST00000504592.5:c.26-10901_26-10898del	ENSP00000421443.1:n.26-10901_26-10898del
ENST00000508653.5:c.70+27957_70+27960del	ENSP00000422314.1:n.70+27957_70+27960del
NM_001083907.2:c.-21+4969_-21+4972del	NP_001077376.2:n.-21+4969_-21+4972del
NM_001127507.2:c.70+27957_70+27960del	NP_001120979.2:n.70+27957_70+27960del
NM_017935.4:c.71-10901_71-10898del	NP_060405.4:n.71-10901_71-10898del
XM_017008337.2:c.-20-10901_-20-10898del	XP_016863826.1:n.-20-10901_-20-10898del
NM_017935.5:c.71-10901_71-10898del MANE Select	NP_060405.5:n.71-10901_71-10898del
NM_001083907.3:c.-21+4969_-21+4972del	NP_001077376.3:n.-21+4969_-21+4972del
NM_001127507.3:c.70+27957_70+27960del	NP_001120979.3:n.70+27957_70+27960del