Canonical Allele Identifier: CA1481132426

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944249_101944250delinsCA , CM000666.2:g.101944249_101944250delinsCA	GRCh38
NC_000004.11:g.102865406_102865407delinsCA , CM000666.1:g.102865406_102865407delinsCA	GRCh37
NC_000004.10:g.103084429_103084430delinsCA	NCBI36
NG_015824.1:g.158643_158644delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+26060_1206+26061delinsCA MANE Select	ENSP00000320509.4:n.1206+26060_1206+26061delinsCA
ENST00000322953.8:c.1206+26060_1206+26061delinsCA	ENSP00000320509.4:n.1206+26060_1206+26061delinsCA
ENST00000428908.5:c.807+26060_807+26061delinsCA	ENSP00000412748.1:n.807+26060_807+26061delinsCA
ENST00000444316.2:c.1116+26060_1116+26061delinsCA	ENSP00000388817.2:n.1116+26060_1116+26061delinsCA
ENST00000504592.5:c.1161+26060_1161+26061delinsCA	ENSP00000421443.1:n.1161+26060_1161+26061delinsCA
ENST00000508653.5:c.807+26060_807+26061delinsCA	ENSP00000422314.1:n.807+26060_807+26061delinsCA
NM_001083907.2:c.1116+26060_1116+26061delinsCA	NP_001077376.2:n.1116+26060_1116+26061delinsCA
NM_001127507.2:c.807+26060_807+26061delinsCA	NP_001120979.2:n.807+26060_807+26061delinsCA
NM_017935.4:c.1206+26060_1206+26061delinsCA	NP_060405.4:n.1206+26060_1206+26061delinsCA
XM_017008337.2:c.1116+26060_1116+26061delinsCA	XP_016863826.1:n.1116+26060_1116+26061delinsCA
NM_017935.5:c.1206+26060_1206+26061delinsCA MANE Select	NP_060405.5:n.1206+26060_1206+26061delinsCA
NM_001083907.3:c.1116+26060_1116+26061delinsCA	NP_001077376.3:n.1116+26060_1116+26061delinsCA
NM_001127507.3:c.807+26060_807+26061delinsCA	NP_001120979.3:n.807+26060_807+26061delinsCA