Canonical Allele Identifier: CA1481132044

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944008_101944012delinsATGTG , CM000666.2:g.101944008_101944012delinsATGTG	GRCh38
NC_000004.11:g.102865165_102865169delinsATGTG , CM000666.1:g.102865165_102865169delinsATGTG	GRCh37
NC_000004.10:g.103084188_103084192delinsATGTG	NCBI36
NG_015824.1:g.158402_158406delinsATGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+25819_1206+25823delinsATGTG MANE Select	ENSP00000320509.4:n.1206+25819_1206+25823delinsATGTG
ENST00000322953.8:c.1206+25819_1206+25823delinsATGTG	ENSP00000320509.4:n.1206+25819_1206+25823delinsATGTG
ENST00000428908.5:c.807+25819_807+25823delinsATGTG	ENSP00000412748.1:n.807+25819_807+25823delinsATGTG
ENST00000444316.2:c.1116+25819_1116+25823delinsATGTG	ENSP00000388817.2:n.1116+25819_1116+25823delinsATGTG
ENST00000504592.5:c.1161+25819_1161+25823delinsATGTG	ENSP00000421443.1:n.1161+25819_1161+25823delinsATGTG
ENST00000508653.5:c.807+25819_807+25823delinsATGTG	ENSP00000422314.1:n.807+25819_807+25823delinsATGTG
NM_001083907.2:c.1116+25819_1116+25823delinsATGTG	NP_001077376.2:n.1116+25819_1116+25823delinsATGTG
NM_001127507.2:c.807+25819_807+25823delinsATGTG	NP_001120979.2:n.807+25819_807+25823delinsATGTG
NM_017935.4:c.1206+25819_1206+25823delinsATGTG	NP_060405.4:n.1206+25819_1206+25823delinsATGTG
XM_017008337.2:c.1116+25819_1116+25823delinsATGTG	XP_016863826.1:n.1116+25819_1116+25823delinsATGTG
NM_017935.5:c.1206+25819_1206+25823delinsATGTG MANE Select	NP_060405.5:n.1206+25819_1206+25823delinsATGTG
NM_001083907.3:c.1116+25819_1116+25823delinsATGTG	NP_001077376.3:n.1116+25819_1116+25823delinsATGTG
NM_001127507.3:c.807+25819_807+25823delinsATGTG	NP_001120979.3:n.807+25819_807+25823delinsATGTG