Canonical Allele Identifier: CA2762858613

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944073_101944074insAA , CM000666.2:g.101944073_101944074insAA	GRCh38
NC_000004.11:g.102865230_102865231insAA , CM000666.1:g.102865230_102865231insAA	GRCh37
NC_000004.10:g.103084253_103084254insAA	NCBI36
NG_015824.1:g.158467_158468insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+25884_1206+25885insAA MANE Select	ENSP00000320509.4:n.1206+25884_1206+25885insAA
ENST00000322953.8:c.1206+25884_1206+25885insAA	ENSP00000320509.4:n.1206+25884_1206+25885insAA
ENST00000428908.5:c.807+25884_807+25885insAA	ENSP00000412748.1:n.807+25884_807+25885insAA
ENST00000444316.2:c.1116+25884_1116+25885insAA	ENSP00000388817.2:n.1116+25884_1116+25885insAA
ENST00000504592.5:c.1161+25884_1161+25885insAA	ENSP00000421443.1:n.1161+25884_1161+25885insAA
ENST00000508653.5:c.807+25884_807+25885insAA	ENSP00000422314.1:n.807+25884_807+25885insAA
NM_001083907.2:c.1116+25884_1116+25885insAA	NP_001077376.2:n.1116+25884_1116+25885insAA
NM_001127507.2:c.807+25884_807+25885insAA	NP_001120979.2:n.807+25884_807+25885insAA
NM_017935.4:c.1206+25884_1206+25885insAA	NP_060405.4:n.1206+25884_1206+25885insAA
XM_017008337.2:c.1116+25884_1116+25885insAA	XP_016863826.1:n.1116+25884_1116+25885insAA
NM_017935.5:c.1206+25884_1206+25885insAA MANE Select	NP_060405.5:n.1206+25884_1206+25885insAA
NM_001083907.3:c.1116+25884_1116+25885insAA	NP_001077376.3:n.1116+25884_1116+25885insAA
NM_001127507.3:c.807+25884_807+25885insAA	NP_001120979.3:n.807+25884_807+25885insAA