Canonical Allele Identifier: CA1481090063

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818670_101818671delinsTA , CM000666.2:g.101818670_101818671delinsTA	GRCh38
NC_000004.11:g.102739827_102739828delinsTA , CM000666.1:g.102739827_102739828delinsTA	GRCh37
NC_000004.10:g.102958850_102958851delinsTA	NCBI36
NG_015824.1:g.33064_33065delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11138_71-11137delinsTA MANE Select	ENSP00000320509.4:n.71-11138_71-11137delinsTA
ENST00000322953.8:c.71-11138_71-11137delinsTA	ENSP00000320509.4:n.71-11138_71-11137delinsTA
ENST00000428908.5:c.70+27720_70+27721delinsTA	ENSP00000412748.1:n.70+27720_70+27721delinsTA
ENST00000444316.2:c.-21+4732_-21+4733delinsTA	ENSP00000388817.2:n.-21+4732_-21+4733delinsTA
ENST00000504592.5:c.26-11138_26-11137delinsTA	ENSP00000421443.1:n.26-11138_26-11137delinsTA
ENST00000508653.5:c.70+27720_70+27721delinsTA	ENSP00000422314.1:n.70+27720_70+27721delinsTA
NM_001083907.2:c.-21+4732_-21+4733delinsTA	NP_001077376.2:n.-21+4732_-21+4733delinsTA
NM_001127507.2:c.70+27720_70+27721delinsTA	NP_001120979.2:n.70+27720_70+27721delinsTA
NM_017935.4:c.71-11138_71-11137delinsTA	NP_060405.4:n.71-11138_71-11137delinsTA
XM_017008337.2:c.-20-11138_-20-11137delinsTA	XP_016863826.1:n.-20-11138_-20-11137delinsTA
NM_017935.5:c.71-11138_71-11137delinsTA MANE Select	NP_060405.5:n.71-11138_71-11137delinsTA
NM_001083907.3:c.-21+4732_-21+4733delinsTA	NP_001077376.3:n.-21+4732_-21+4733delinsTA
NM_001127507.3:c.70+27720_70+27721delinsTA	NP_001120979.3:n.70+27720_70+27721delinsTA