Canonical Allele Identifier: CA1481132157
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101944037_101944043delinsTGTGAGA , CM000666.2:g.101944037_101944043delinsTGTGAGA GRCh38
NC_000004.11:g.102865194_102865200delinsTGTGAGA , CM000666.1:g.102865194_102865200delinsTGTGAGA GRCh37
NC_000004.10:g.103084217_103084223delinsTGTGAGA NCBI36
NG_015824.1:g.158431_158437delinsTGTGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.1206+25848_1206+25854delinsTGTGAGA MANE Select ENSP00000320509.4:n.1206+25848_1206+25854delinsTGTGAGA
ENST00000322953.8:c.1206+25848_1206+25854delinsTGTGAGA ENSP00000320509.4:n.1206+25848_1206+25854delinsTGTGAGA
ENST00000428908.5:c.807+25848_807+25854delinsTGTGAGA ENSP00000412748.1:n.807+25848_807+25854delinsTGTGAGA
ENST00000444316.2:c.1116+25848_1116+25854delinsTGTGAGA ENSP00000388817.2:n.1116+25848_1116+25854delinsTGTGAGA
ENST00000504592.5:c.1161+25848_1161+25854delinsTGTGAGA ENSP00000421443.1:n.1161+25848_1161+25854delinsTGTGAGA
ENST00000508653.5:c.807+25848_807+25854delinsTGTGAGA ENSP00000422314.1:n.807+25848_807+25854delinsTGTGAGA
NM_001083907.2:c.1116+25848_1116+25854delinsTGTGAGA NP_001077376.2:n.1116+25848_1116+25854delinsTGTGAGA
NM_001127507.2:c.807+25848_807+25854delinsTGTGAGA NP_001120979.2:n.807+25848_807+25854delinsTGTGAGA
NM_017935.4:c.1206+25848_1206+25854delinsTGTGAGA NP_060405.4:n.1206+25848_1206+25854delinsTGTGAGA
XM_017008337.2:c.1116+25848_1116+25854delinsTGTGAGA XP_016863826.1:n.1116+25848_1116+25854delinsTGTGAGA
NM_017935.5:c.1206+25848_1206+25854delinsTGTGAGA MANE Select NP_060405.5:n.1206+25848_1206+25854delinsTGTGAGA
NM_001083907.3:c.1116+25848_1116+25854delinsTGTGAGA NP_001077376.3:n.1116+25848_1116+25854delinsTGTGAGA
NM_001127507.3:c.807+25848_807+25854delinsTGTGAGA NP_001120979.3:n.807+25848_807+25854delinsTGTGAGA