Canonical Allele Identifier: CA1481088938
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101816134_101816135delinsGT , CM000666.2:g.101816134_101816135delinsGT GRCh38
NC_000004.11:g.102737291_102737292delinsGT , CM000666.1:g.102737291_102737292delinsGT GRCh37
NC_000004.10:g.102956314_102956315delinsGT NCBI36
NG_015824.1:g.30528_30529delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.71-13674_71-13673delinsGT MANE Select ENSP00000320509.4:n.71-13674_71-13673deli...
ENST00000322953.8:c.71-13674_71-13673delinsGT ENSP00000320509.4:n.71-13674_71-13673deli...
ENST00000428908.5:c.70+25184_70+25185delinsGT ENSP00000412748.1:n.70+25184_70+25185deli...
ENST00000444316.2:c.-21+2196_-21+2197delinsGT ENSP00000388817.2:n.-21+2196_-21+2197deli...
ENST00000504592.5:c.26-13674_26-13673delinsGT ENSP00000421443.1:n.26-13674_26-13673deli...
ENST00000508653.5:c.70+25184_70+25185delinsGT ENSP00000422314.1:n.70+25184_70+25185deli...
NM_001083907.2:c.-21+2196_-21+2197delinsGT NP_001077376.2:n.-21+2196_-21+2197delinsG...
NM_001127507.2:c.70+25184_70+25185delinsGT NP_001120979.2:n.70+25184_70+25185delinsG...
NM_017935.4:c.71-13674_71-13673delinsGT NP_060405.4:n.71-13674_71-13673delinsGT
XM_017008337.2:c.-20-13674_-20-13673delinsGT XP_016863826.1:n.-20-13674_-20-13673delin...
NM_017935.5:c.71-13674_71-13673delinsGT MANE Select NP_060405.5:n.71-13674_71-13673delinsGT
NM_001083907.3:c.-21+2196_-21+2197delinsGT NP_001077376.3:n.-21+2196_-21+2197delinsG...
NM_001127507.3:c.70+25184_70+25185delinsGT NP_001120979.3:n.70+25184_70+25185delinsG...