Canonical Allele Identifier: CA1481088973
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101816190_101816191delinsTA , CM000666.2:g.101816190_101816191delinsTA GRCh38
NC_000004.11:g.102737347_102737348delinsTA , CM000666.1:g.102737347_102737348delinsTA GRCh37
NC_000004.10:g.102956370_102956371delinsTA NCBI36
NG_015824.1:g.30584_30585delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.71-13618_71-13617delinsTA MANE Select ENSP00000320509.4:n.71-13618_71-13617delinsTA
ENST00000322953.8:c.71-13618_71-13617delinsTA ENSP00000320509.4:n.71-13618_71-13617delinsTA
ENST00000428908.5:c.70+25240_70+25241delinsTA ENSP00000412748.1:n.70+25240_70+25241delinsTA
ENST00000444316.2:c.-21+2252_-21+2253delinsTA ENSP00000388817.2:n.-21+2252_-21+2253delinsTA
ENST00000504592.5:c.26-13618_26-13617delinsTA ENSP00000421443.1:n.26-13618_26-13617delinsTA
ENST00000508653.5:c.70+25240_70+25241delinsTA ENSP00000422314.1:n.70+25240_70+25241delinsTA
NM_001083907.2:c.-21+2252_-21+2253delinsTA NP_001077376.2:n.-21+2252_-21+2253delinsTA
NM_001127507.2:c.70+25240_70+25241delinsTA NP_001120979.2:n.70+25240_70+25241delinsTA
NM_017935.4:c.71-13618_71-13617delinsTA NP_060405.4:n.71-13618_71-13617delinsTA
XM_017008337.2:c.-20-13618_-20-13617delinsTA XP_016863826.1:n.-20-13618_-20-13617delinsTA
NM_017935.5:c.71-13618_71-13617delinsTA MANE Select NP_060405.5:n.71-13618_71-13617delinsTA
NM_001083907.3:c.-21+2252_-21+2253delinsTA NP_001077376.3:n.-21+2252_-21+2253delinsTA
NM_001127507.3:c.70+25240_70+25241delinsTA NP_001120979.3:n.70+25240_70+25241delinsTA