Canonical Allele Identifier: CA2519520887

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818954_101818955insTATTAATAAAATAG , CM000666.2:g.101818954_101818955insTATTAATAAAATAG	GRCh38
NC_000004.11:g.102740111_102740112insTATTAATAAAATAG , CM000666.1:g.102740111_102740112insTATTAATAAAATAG	GRCh37
NC_000004.10:g.102959134_102959135insTATTAATAAAATAG	NCBI36
NG_015824.1:g.33348_33349insTATTAATAAAATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10854_71-10853insTATTAATAAAATAG MANE Select	ENSP00000320509.4:n.71-10854_71-10853insTATTAATAAAATAG
ENST00000322953.8:c.71-10854_71-10853insTATTAATAAAATAG	ENSP00000320509.4:n.71-10854_71-10853insTATTAATAAAATAG
ENST00000428908.5:c.70+28004_70+28005insTATTAATAAAATAG	ENSP00000412748.1:n.70+28004_70+28005insTATTAATAAAATAG
ENST00000444316.2:c.-21+5016_-21+5017insTATTAATAAAATAG	ENSP00000388817.2:n.-21+5016_-21+5017insTATTAATAAAATAG
ENST00000504592.5:c.26-10854_26-10853insTATTAATAAAATAG	ENSP00000421443.1:n.26-10854_26-10853insTATTAATAAAATAG
ENST00000508653.5:c.70+28004_70+28005insTATTAATAAAATAG	ENSP00000422314.1:n.70+28004_70+28005insTATTAATAAAATAG
NM_001083907.2:c.-21+5016_-21+5017insTATTAATAAAATAG	NP_001077376.2:n.-21+5016_-21+5017insTATTAATAAAATAG
NM_001127507.2:c.70+28004_70+28005insTATTAATAAAATAG	NP_001120979.2:n.70+28004_70+28005insTATTAATAAAATAG
NM_017935.4:c.71-10854_71-10853insTATTAATAAAATAG	NP_060405.4:n.71-10854_71-10853insTATTAATAAAATAG
XM_017008337.2:c.-20-10854_-20-10853insTATTAATAAAATAG	XP_016863826.1:n.-20-10854_-20-10853insTATTAATAAAATAG
NM_017935.5:c.71-10854_71-10853insTATTAATAAAATAG MANE Select	NP_060405.5:n.71-10854_71-10853insTATTAATAAAATAG
NM_001083907.3:c.-21+5016_-21+5017insTATTAATAAAATAG	NP_001077376.3:n.-21+5016_-21+5017insTATTAATAAAATAG
NM_001127507.3:c.70+28004_70+28005insTATTAATAAAATAG	NP_001120979.3:n.70+28004_70+28005insTATTAATAAAATAG